Compositions isolated from bovine mammary gland and methods for their use

ABSTRACT

Isolated polynucleotides encoding polypeptides expressed in bovine mammary gland tissue are provided, together with genetic constructs and host cells comprising such isolated polynucleotides. Methods for the use of such polynucleotides and polypeptides are also provided.

CROSS-REFERENCE TO RELATED APPLICATIONS

[0001] This application is a continuation of U.S. patent application Ser. No. 09/644,265, filed Aug. 22, 2000, which claims priority to U.S. Provisional Patent Application No. 60/150,330, filed Aug. 23, 1999.

TECHNICAL FIELD OF THE INVENTION

[0002] This invention relates to polypeptides expressed in bovine mammary gland cells, polynucleotides encoding such polypeptides and methods for treating a mammal involving administration of a polypeptide or polynucleotide of the present invention.

BACKGROUND OF THE INVENTION

[0003] The bovine mammary gland is a milk-producing organ of great economic importance. Knowledge of the genes expressed in this tissue is valuable in understanding the physiology and function of the mammary gland, not only in the cow, but also in other mammals, including humans. The polynucleotide sequences themselves are useful in detecting the presence of mammary gland tissue in a biological sample, and in the development of transgenic animals with transgene expression targeted to the mammary gland, e.g., by using mammary gland-specific promoters isolated from mammary-specific polynucleotides.

SUMMARY OF THE INVENTION

[0004] The present invention provides isolated polypeptides expressed in bovine mammary gland cells and isolated polynucleotides encoding such polypeptides, together with genetic constructs and host cells comprising such polynucleotides. Methods for using such polypeptides, polynucleotides and genetic constructs are also provided.

[0005] In specific embodiments, isolated polynucleotides are provided that comprise a polynucleotide sequence selected from the group consisting of: (a) sequences recited in SEQ ID NOS: 1-68; (b) complements of the sequences recited in SEQ ID NOS: 1-68; (c) reverse complements of the sequences recited in SEQ ID NOS: 1-68; (d) reverse sequences of the sequences recited in SEQ ID NOS: 1-68; (e) sequences having a 99% probability of being to the same as a sequence of (a)-(d), determined as described below; and (f) sequences having at least 75%, 90% or 95% identity to a sequence of (a)-(d), the percentage identity being determined as described below. Polynucleotides comprising at least a specified number of contiguous residues (“x-mers”) of any of the sequences identified as SEQ ID NOS: 1-68 are also provided, together with extended sequences, and oligonucleotide probes and primers corresponding to the sequences set out in SEQ ID NOS: 1-68. All of these polynucleotides and oligonucleotide probes and primers are collectively referred to herein as “polynucleotides of the present invention”.

[0006] In further embodiments, the present invention provides isolated polypeptides comprising an amino acid sequence encoded by a polynucleotide selected from the group consisting of: (a) sequences provided in SEQ ID NOS: 1-68; and (b) sequences having at least 75%, 90% or 95% identity to a sequence provided in SEQ ID NOS: 1-68, together with isolated polynucleotides encoding such polypeptides. Isolated polypeptides comprising at least a functional portion of a polypeptide comprising an amino acid sequence encoded by a polynucleotide selected from the group consisting of: (a) sequences provided in SEQ ID NOS: 1-68; and (b) sequences having 75%, 90% or 95% identity to a sequence of SEQ ID NOS: 1-68, are also provided. In certain specific embodiments, the inventive polypeptides comprise an amino acid sequence selected from the group consisting of sequences identified as SEQ ID NOS: 69-136, and variants thereof.

[0007] In related embodiments, the present invention provides genetic constructs comprising the above polynucleotides, together with host cells transformed with such constructs, and organisms comprising such host cells.

[0008] In a further aspect, the present invention provides methods for stimulating bovine mammary gland cell growth and function, inhibiting the growth of various mammary gland cancer cells, inhibiting angiogenesis and vascularization of tumors, or modulating the growth of blood vessels in a mammal, such methods comprising administering to the subject a composition comprising an isolated polypeptide of the present invention. Methods for modulating mammary gland function in a mammal are also provided, the methods comprising administering to the subject a composition comprising an inventive polypeptide.

[0009] As detailed below, the isolated polynucleotides and polypeptides of the present invention may be usefully employed in the preparation of therapeutic agents for the treatment of mammary gland disorders. In addition, polynucleotides that are specifically expressed at a higher or lower level in diseased mammary gland than in a normal mammary gland may be used as an indicator of the disease condition. Similarly, disposition to a disease related to a specific level of expression of a polynucleotide would indicate use of that polynucleotide as a marker for diagnosis of susceptible individuals. In yet another aspect, the mapping of a specific polynucleotide of this invention close to the chromosomal location of any beneficial or detrimental genes would make the polynucleotide a valuable tool for breeding of livestock, disease diagnostics, or identification of the beneficial or detrimental gene.

[0010] The isolated polynucleotides of the present invention have further utility in genome mapping, in physical mapping, and in positional cloning of genes. Additionally, the polynucleotide sequences identified as SEQ ID NOS: 1-68, and their variants, may be used to design oligonucleotide probes and primers (referred to collectively as “oligonucleotides”). As detailed below, oligonucleotide probes and primers have sequences that are substantially complementary to the polynucleotide of interest over a certain portion of the polynucleotide. The inventive oligonucleotide probes may be used to detect the presence, and examine the expression patterns, of genes in any organism having sufficiently similar DNA and RNA sequences in their cells using techniques that are well known in the art, such as slot blot DNA hybridization techniques. The inventive oligonucleotide primers may be used for PCR amplifications. Oligonucleotide probes and primers of the present invention may also be used in connection with various microarray technologies, including the microarray technology of Affymetrix, Inc. (Santa Clara, Calif.).

[0011] The above-mentioned and additional features of the present invention, together with the manner of obtaining them, will be best understood by reference to the following more detailed description. All references disclosed herein are incorporated herein by reference in their entirety as if each was incorporated individually.

DETAILED DESCRIPTION OF THE INVENTION

[0012] In certain aspects, the present invention provides polynucleotides that were isolated by sequencing of cDNA libraries from bovine mammary gland cells, together with polypeptides encoded by such polynucleotides.

[0013] The polynucleotides of the present invention encode polypeptides that have important roles in growth, development and function of mammary gland cells, and in responses of mammary gland cells to tissue injury and inflammation, as well as disease states, and which have antibacterial or other bioactive utility. The polypeptides and/or polynucleotides of the present invention may thus be employed in the modification of mammary function, as potential markers for selection of livestock having enhanced mammary performance, and as diagnostics for abnormal cellular growth in mammary cancer. Oligonucleotide probes and primers corresponding to the inventive polynucleotides may be employed to detect the presence of mammary gland tissue in a specific tissue sample using techniques well known in the art, such as DNA hybridization and polymerase chain reaction (PCR) amplification.

[0014] The inventive polypeptides have important roles in processes such as induction of mammary growth, differentiation of milk producing cells, cell migration, cell proliferation, and cell-cell interaction. The polypeptides are important in the maintenance of tissue integrity, and thus are important in processes such as wound healing. Some of the disclosed polypeptides can act as modulators of immune responses, especially since milk is known to contain immunologically active polypeptides for the benefit of mammal offspring. In addition, many polypeptides are immunologically active also within the mammary gland, making them important therapeutic targets in a whole range of disease states not only within the mammary gland, but also in other tissues of a mammal. Antibodies to the polypeptides of the present invention and small molecule inhibitors related to the polypeptides of the present invention may also be used for modulating immune responses and for treatment of diseases according to the present invention.

[0015] The isolated polynucleotides and polypeptides of the present invention have demonstrated similarity to polynucleotides and/or polypeptides of known function. The putative identity and functions of the inventive polynucleotides based on such similarities are shown in Table 1. TABLE 1 SEQ SEQ ID NO: ID NO: Poly- Poly- nucleotide peptide Category Related gene function or protein class  1  69 Cell signaling/ Hepatocellular carcinoma and breast cancer associated Differentiation protein.  2  70 Cell signaling/Cell Platelet glycoprotein IV, CD36 antigen or PAS-4 protein, surface antigen has numerous potential physiological functions. It binds to collagen, thrombospondin, anionic phospholipids and oxidized LDL, and functions as a cell adhesion molecule. Directly mediates cytoadherence of Plasmodium falciparum parasitized erythrocytes, binds long chain fatty acids and functions in the transport and/or as a regulator of fatty acid transport.  3  71 Cell signaling/Cell T-cell receptor T3 delta chain is part of the CD3 complex surface antigen that mediates signal transduction.  4  72 Cell signaling/ Entactin-2 or nidogen-2, is a cell adhesion glycoprotein Differentiation that is involved in osteoblast differentiation. It has a role in cell- extracellular matrix interactions.  5  73 Cell signaling/ Myotrophin, granule cell differentiation protein or v-1 Differentiation protein has a role in cerebellar morphogenesis and functions in differentiation of cerebellar neurons, particularly of granule cells. It is normally expressed at the completion of differentiation and migration of granular cells and at the initiation of the formation of synapses in cerebellar neurons.  6  74 Cell signaling/ Novel abundant testis protein TEGT Differentiation  7  75 Cell signaling/ Connective tissue growth factor is the major connective Growth factor tissue mitoattractant secreted by human vascular endothelial cells. This immediate-early protein binds one of the PDGF cell surface receptors. It belongs to the insulin-like growth factor binding protein family.  8  76 Intracellular cell Adenomatosis polyposis coli binding protein EB1 (APC- signaling binding) is involved in the mechanism through which APC suppresses colonic neoplasia.  9  77 Intracellular cell Adenylyl cyclase-associated protein 1 (CAP 1), is a signaling mammalian homologue of the yeast protein that associates with adenylyl cyclase and thereby enables adenylyl cyclase to respond appropriately to upstream regulatory signals. 10  78 Intracellular cell AMSH - associated molecule with the SH3 domain of signaling STAM (signal transducing adaptor molecule), which is tyrosine-phosphorylated downstream of Jak2 and Jak3 after stimulation with various cytokines such a IL-2, IL-3, IL-4, IL-7, GM- CSF, EGF and PDGF. STAM contains an SH3 (Src-homology 3) domain and the ITAM (immunoreceptor tyrosine-based activation motif), and therefore STAM acts as an adaptor molecule involved in signal transducing pathways from the cytokine receptors. AMSH appears to play a critical role in the cytokine- mediated intracellular signal transduction downstream of the Jak2/Jak3.STAM complex. 11  79 Intracellular cell Nel-like protein 2, is a homotrimer that binds to PKC signaling beta-1. It contain several protein motifs including a secretion signal peptide, an NH(2)-terminal thrombospondin-1 (TSP-1)-like module, five von Willebrand factor C domains, and six epidermal growth factor-like domains. It is strongly expressed in early embryonic neural tissues (brain, spinal cord, and dorsal root ganglia); less in other tissues such as cells around cartilage, myocardium, lung mesenchymal cells, and liver. 12  80 Intracellular cell Peroxisomal targeting signal 2 receptor binds to the N- signaling terminal PTS2-type peroxisomal targeting signal and plays an essential role in peroxisomal protein import. Interacts with PEX5. 13  81 Intracellular cell Peroxisome proliferator-activated receptor binding signaling protein, also known as thyroid hormone receptor- associated protein complex component, TRAP 220, thyroid receptor interacting protein 2, TRIP2, or p53 regulatory protein, RB 18a, interacts with thyroid hormone receptors. to regulate nuclear receptor-mediated transcription. The protein binds DNA and p53 protein. 14  82 Intracellular cell Retinoblastoma binding protein identified as a signaling differentially expressed gene in activation of the transforming growth factor-beta signal transduction pathway in mammary carcinomas treated with the anticancer monoterpenes 15  83 Intracellular cell Silencer of death domains (SODD), is a widely signaling expressed, approximately 60-kilodalton protein, that was found to be associated with the death domain of TNF-R1. TNF treatment released SODD from TNF-RI, permitting the recruitment of proteins such as TRADD and TRAF2 to the active TNF-R1 signaling complex. SODD also interacts with death receptor-3 (DR3), another member of the TNF receptor superfamily and SODD association may be representative of a general mechanism for preventing spontaneous signaling by death domain-containing receptors. 16  84 Cell signaling/ Pigment epithelium-derived factor is a neurotrophic Differentiation protein that induces extensive neuronal differentiation in retinoblastoma cells. Although it belongs to the serpin family, it does not undergo the S (stressed) to R (relaxed) conformational transition characteristic of active serpins and it exhibits no serine protease inhibitory activity. The N-terminal (aa 42-139) exhibits neurite outgrowth- inducing activity. The C-terminal exposed loop (aa 380- 416) is essential for serpin activity. 17  85 Intracellular cell HSP90 Molecular chaperone with ATPase activity. signaling Belongs to the heat shock protein 90 family. 18  86 Cell signaling/Cell Peanut-like protein 2, brain protein H5, surface antigen is involved in cytokinesis. It belongs to the CDC3/CDC10/CDC11/CDC12 family. 19  87 Cell structure/ Keratin, type I cytoskeletal 17, (K17) is a marker of basal Cytoskeleton cell differentiation in complex epithelia and therefore indicative of a certain type of epithelial “stem cells”. There are two types of cytoskeletal and microfibrillar keratin: I (acidic; 40-55 kDa) [K9 to K20] and II (neutral to basic; 56-70 kDa) [K1 to K8]. Both a basic and an acidic keratin are required for filament assembly. Expressed in the hair follicle, nail bed, mucosal stratified squamous epithelia and in basal cells of oral epithelium, palmoplantar epidermis and sweat and mammary glands. K17 is induced in damaged or stressed epidermis. K16 and K17 are coexpressed only in pathological situations such as metaplasias and carcinomas of the uterine cervix and in psoriasis vulgaris. Defects in K17 have been found to be associated with type II pachyonychia congenita (PC) also known as Jackson-Lawler (J&L) syndrome. Type II PC is characterized by onchyogryposis, limited plantar hyperkeratosis, multiple epidermal cysts. 20  88 Cell structure/ Mesothelial keratin K7 (type II) is similar to all other Cytoskeleton intermediate filament proteins. 21  89 Immune Zn-alpha2-glycoprotein appears to be a truncated modulation/MHC secretory major histocompatibility complex-related molecule, and it may have a role in the expression of the immune response. 22  90 Immune Ig lambda C region encodes the light chain of the IgG modulation/ complex which is the major immunoglobulin found in Antigen receptor colostrum and milk of cows. 23  91 Immune Ig gamma-2 chain C region is the heavy chain of the IgG modulation/ complex that is the major antibody class secreted in Antigen receptor colostrum and milk of cows. 24  92 Immune Ig gamma-2 chain C region is the heavy chain of the IgG modulation/ complex that is the major antibody class secreted in Antigen receptor colostrum and milk of cows. 25  93 Metabolic/ GTP cyclohydrolase I feedback regulatory protein Cofactor synthesis mediates tetrahydrobiopterin inhibition of GTP cyclohydrolase I which catalyses the first step in the biosynthesis of tetrahydrofolate. This inhibition is reversed by L-phenylalanine. 26  94 Metabolic/Iron Lactoferrin or lactotransferrin belongs to the transferrin binding family. Transferrins are iron binding transport proteins which can bind two atoms of ferric iron in association with the binding of an anion, usually bicarbonate. Lactoferrin and peptides derived therefrom such as lactoferricin b have antimicrobial properties. 27  95 Metabolic/Lactose N-acetyllactosamine synthase, N-acetylglucosamine (beta synthesis 1-4) galactosyltransferase or lactose synthase A protein, responsible for the synthesis of complex-type N-linked oligosaccharides in many glycoproteins a as well as the carbohydrate moieties of glycolipids. However in the presence of alpha-lactalbumin, it catalyses the reaction: UDP-galactose + D-glucose = UDP + lactose. 28  96 Metabolic/Lipase Lipoprotem lipase hydrolyses triglycerides of circulating chylomicrons and very low-density lipoproteins (VLDL). The enzyme functions in the presence of apolipoprotein C-2 on the luminal surface of vascular endothelium. It is attached to the membrane by a GPI-anchor. 29  97 Metabolic/ Antioxidant enzyme B166 represents a new mammalian Oxidation subfamily of AhpC/TSA peroxiredoxin antioxidant enzymes with peroxidase activity, and an antioxidant activity comparable with that of catalase. The protein has mitochondrial and peroxisomal targeting sequences. Acute inflammation induced in rat lung by lipopolysaccharide is associated with an increase of B166 mRNA levels in lung, suggesting a protective role for B166 in oxidative and inflammatory processes. 30  98 Metabolic/Purine Purine nucleoside phosphorylase, also known as inosine metabolism phosphorylase, removes phosphates from purine nucleosides 31  99 Metabolic/Purine Bifunctional purine biosynthesis protein, PURH, or 5- synthesis aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase catalyses steps 9 and 10 in the purine synthesis pathway. 32 100 Metabolic/ Glutathione S-transferase P catalyses the conjugation of Xenobiotics reduced glutathione to a wide number of exogenous and endogenous hydrophobic electrophiles. 33 101 Metabolic/ Microsomal glutathione S-transferase 3 is an integral Xenobiotics microsomal membrane protein. It is predominantly expressed in heart, skeletal muscle, and adrenal cortex. Also found in brain, placenta, liver, kidney, pancreas, thyroid, testis, and ovary. Almost absent in lung, thymus, and peripheral blood leukocytes. It appears to be a member of a family that incudes 5-Lipoxygenase activating protein (FLAP), leukotriene-C4 (LTC4) synthase, and microsomal glutathione S-transferase II (microsomal GST-II) and possibly microsomal GST-I. 34 102 Protein synthesis/ Small nuclear ribonucleoprotein SM d2 (SNRNP core mRNA processing protein d2; AM-d2) is involved in mRNA processing. 35 103 Protein synthesis/ Spliceosome associated protein 145 is a subunit of the mRNA processing SF3b complex required for ‘A’ complex assembly formed by the stable binding of U2 SNRNP to the branchpoint sequence (BPS) in pre-mRNA. Sequence independent binding of Sf3a/Sf3b complex upstream of the branch site is essential, it may anchor U2 SNRNP to the pre-mRNA 36 104 Protein synthesis/ Translocon-associated protein, delta subunit precursor Processing (Trap-delta). Trap proteins are part of a complex whose function is to bind Ca(2+) to the endoplasmic reticulum (ER) membrane and thereby regulate the retention of ER resident proteins. 37 105 Protein synthesis/ Translocon-associated protein, delta subunit precursor Processing (Trap-delta). Trap proteins are part of a complex whose function is to bind Ca(2+) to the endoplasmic reticulum (ER) membrane and thereby regulate the retention of ER resident proteins. 38 106 Protein synthesis/ Associates with proteins of the secretory pathway, Secretion suggesting possible role in the early secretory pathway. Central and C-terminal regions exhibit significant homology to phospholipid-modifying proteins, especially phosphatidic acid preferring-phospholipase A1. 39 107 Protein synthesis/ Pancreatic zymogen granule membrane protein GP-2 is Secretion attached to the membrane by a GPI-anchor, then cleaved to produce a soluble form which is secreted in pancreatic juice. 40 108 Protein synthesis/ E74-like factor 5, ELF5, is a novel transcription factor Transcription that belongs to the ELF subfamily of ETS genes and maps to human chromosome 11p13-15, a region subject to LOH and rearrangement in human carcinoma cell lines. 41 109 Protein synthesis/ ERGB is a member of the family of human ETS Transcription transcription factors and shows extensive amino acid identity to the human ERG and the mouse Fli-1 genes. The ERGB gene is found to be transcriptionally active in a variety of human cell lines and tissues, in contrast to the more restrictive expression pattern of the ERG gene. 42 110 Protein synthesis/ ESE-2 is a novel ESE-l-related Ets transcription factor Transcription that is restricted to glandular epithelium and differentiated keratinocytes. 43 111 Protein synthesis/ Identified as a liver-specific human protein that is 62% Transcription identical to IQGAP1 and proposed to play role in the CDC42 and Rac1 controlled generation of specific actin structures. 44 112 Protein synthesis/ Nuclear factor erythroid 2 related factor 2 may be Transcription involved in the transcriptional activation of genes of the beta-globin cluster by mediating enhancer activity of hypersensitive site 2 of the beta-globin locus control region. 45 113 Protein synthesis/ Transcription initiation factor TFIId 31 kDa subunit is a Transcription component of the transcription factor IId (TFIId) complex that is essential for mediating regulation of RNA polymerase transcription. TAFII31 is a coactivator for the p53 protein. Also interacts with the acidic transactivator viral protein 16 (VP16) as well as with the general transcription factor TFIIb. 46 114 Protein synthesis/ Eukaryotic translation initiation factor 4b (eIF4-b)is Translation required for the binding of mRNA to ribosomes. Functions in close association with eIF4-f and eIF4-a. Binds near the 5′-terminal cap of mRNA in presence of eIF4-f and ATP. Promotes the ATPase activity and the ATP-dependent RNA unwinding activity of both eIF4-a and eIF4-f 47 115 Protein synthesis/ FK506-binding protein, peptidyl-prolyl cis-trans Translation isomerase, belongs to the FKBP-type PPIase family. PPIases accelerate the folding of proteins through the cis- trans isomerization of proline imidic peptide bonds in oligopeptides. 48 116 Protein synthesis/ Human protein, Pin1, is an essential peptidyl-prolyl Translation cis/trans isomerase (PPIase) that interacts with NIMA and attenuates its mitosis-promoting activity. PPIases are important in protein folding, assembly and/or transport. 49 117 Protein Glycyl-tRNA synthetase (ec 6.1.1.14) (glycine-tRNA synthesis/tRNA ligase) (GLYS) catalyses the synthesis of glycyl-tRNA. synthesis 50 118 Protein turnover/ Proteasome subunit C7-I is part of the 20S proteasome Proteasome involved in the intracellular turnover of proteins tagged as pan of the ubiquitin pathway. 51 119 Protein synthesis/ Chromosome associated polypeptide-3, homologous to Transcription Xenopus laevis XCAP-C. 52 120 Protein turnover/ Ubiquitin binds to protein to tag them for intracellular Proteasome degradation by the proteasome system and for other metabolic processes. 53 121 Cell signaling/ Cell cycle protein is a potential cell division regulator. Differentiation 54 122 Immune Cathepsin F is a cysteine protease and a member of the modulation/ papain family that has a role in the processing of the Antigen processing invariant chain processing and MHC class II peptide loading by macrophages. 55 123 Immune High affinity immunoglobulin gamma Fc receptor I binds modulation/ to the Fc region of immunoglobulin gamma and is Antibody uptake responsible for the uptake of IgG molecules and important in the transfer of IgG molecules across mammuary epithelia. 56 124 Metabolic/ Fumarate hydratase, mitochondrial precursor (ec 4.2.1.2) Oxidation (fumarase) catalyses a step in the citric acid cycle. 57 125 Cell signaling/ Lipophilin b is a secreted protein of the uteroglobin Differentiation family that binds androgens and other steroids, also binds estramustine, a chemotherapeutic agent used for prostate cancer. Thought to be under transcriptional regulation of steroid hormones. Highest expression is found in skeletal muscle, but also expressed in thymus, trachea, kidney, steroid responsive tissues (prostate, testis, uterus, breast and ovary), and salivary gland. 58 126 Immune High affinity immunoglobulin gamma Fc receptor I binds modulation/ to the Fc region of immunoglobulin gamma and is Antibody uptake responsible for the uptake of IgG molecules and important in the transfer of IgG molecules across mammary epithelia. 59 127 Cell signaling/ B Cell translocation gene 1 (BTG1) is a member of a Differentiation family of putative antiproliferative factors. They are characterized by their rapid, but transient, expression in response to factors that induce growth arrest and subsequent differentiation. 60 128 Protein synthesis/ LSM3 protein is involved in mRNA processing. Translation 61 129 Protein synthesis/ CTCF is a highly evolutionarily conserved 11-zinc finger Transcription transcriptional factor possessing multiple DNA sequence specificity. CTCF binds to a number of important regulatory within the 5′ non-coding sequence of the human MYC oncogene, and it can regulate its transcription in several experimental systems. CTCF mRNA is expressed in cells of multiple different lineages. Enforced ectopic expression of CTCF inhibits cell growth in culture. 62 130 Cell signaling/ Intestinal trefoil factor is a secreted protein that has a Differentiation potential role in promoting cell migration. Expressed by goblet cells of small and large epithelia and also by the uterus. 63 131 Metabolic/Lipid Choline and ethanolamine kinase catalyses the synthesis phosphorylation of choline and ethanolamine, a step required for phospholipid synthesis. 64 132 Metabolic/ ATP-binding cassette protein M-ABC1 is a member of Xenobiotics the ATP-binding cassette (ABC) superfamily that is involved in the transport of diverse substrates across organellar and plasma membranes of the mammalian cell. 65 133 Cell signaling/ Negative growth-regulatory protein myd118, also known Differentiation as growth arrest and DNA-damage-inducible protein GADD45 beta, is involved in the regulation of growth and apoptosis. Mediates activation of stress-responsive MTK1/MEKK4 MAPKKK. 66 134 Protein synthesis/ The human BTF2 (TFIIH) transcription factor is a Transcription multisubunit protein involved in transcription initiation by RNA polymerase II(B) as well as in DNA repair. 67 135 Immune Ig light chain is a component of the IgG complex, the modulation/ major immunoglobulin secreted in colostrum and milk Antigen receptor 68 136 Transcription Retinoic acid receptor responder protein 2, tazarotene- factor induced gene 2 protein or RAR-responsive protein tig2 is highly expressed in skin (basal and suprabasal layers of the epidermis, hair follicles and endothelial cells), and is also found in pancreas, liver, spleen, prostate, ovary, small intestine and colon. This protein is inhibited in psoriatic lesions and activated by tazarotene in skin grafts and in the epidermis of psoriatic lesions.

[0016] The polynucleotides of SEQ ID NO: 1-7, 16, 18, 53, 57, 59, 62 and 65 encode polypeptides involved in cell signalling at the extracellular level including both secreted polypeptides and cell surface receptors for secreted polypeptides. These function in regulating cell metabolism and cell growth. The polynucleotides of SEQ ID NO: 1, 4-6, 16, 53, 57, 59, 62 and 65 encode polypeptides that are involved in cellular differentiation. The polynucleotides of SEQ ID NO: 8-15 and 17 encode polypeptides that are intracellular mediators of external cell signalling events. The polynucleotides of SEQ ID NO: 19 and 20 encode polypeptides that are part of the cellular cytoskeleton and that have utility in the manipulation of mammary epithelial cell structure and function. The polynucleotides of SEQ ID NO: 21-24, 54, 55, 58 and 67 encode components of the immune system and have utility in enhancing the concentration of immune proteins in mammary secretions. The polynucleotides of SEQ ID NO: 25-33, 56, 63 and 64 encode polypeptides involved in intracellular metabolic pathways relating to the synthesis and degradation of lipids, carbohydrates and purines, and the oxidation of xenobiotics. The polynucleotides of SEQ ID NO: 34-52, 60, 61 and 66 encode polypeptides that are involved in protein synthesis and degradation. They include transcription factors that regulate mRNA synthesis, and polypeptides involved in the transcription process, the processing of mRNA, the translation of mRNA to produce polypeptides and processing and turnover of specific proteins. These polynucleotides have utility in the manipulation of the synthesis of mammary secretions to modify the yields of milk and specific milk proteins.

[0017] Isolated polynucleotides of the present invention include the polynucleotides identified herein as SEQ ID NOS: 1-68; isolated polynucleotides comprising a polynucleotide sequence selected from the group consisting of SEQ ID NOS: 1-68; isolated polynucleotides comprising at least a specified number of contiguous residues (x-mers) of any of the polynucleotides identified as SEQ ID NOS: 1-68; isolated polynucleotides comprising a polynucleotide sequence that is complementary to any of the above polynucleotides; isolated polynucleotides comprising a polynucleotide sequence that is a reverse sequence or a reverse complement of any of the above polynucleotides; antisense sequences corresponding to any of the above polynucleotides; and variants of any of the above polynucleotides, as that term is described in this specification.

[0018] The definition of the terms “complement,” “reverse complement,” and “reverse sequence,” as used herein, is best illustrated by the following example. For the sequence 5′ AGGACC 3′, the complement, reverse complement, and reverse sequence are as follows: complement 3′ TCCTGG 5′ reverse complement 3′ GGTCCT 5′ reverse sequence 5′ CCAGGA 3′.

[0019] Preferably, sequences that are complements of a specifically recited polynucleotide sequence are complementary over the entire length of the specific polynucleotide sequence.

[0020] As used herein, the term “oligonucleotide” refers to a relatively short segment of a polynucleotide sequence, generally comprising between 6 and 60 nucleotides, and comprehends both probes for use in hybridization assays and primers for use in the amplification of DNA by polymerase chain reaction.

[0021] As used herein, the term “polynucleotide” means a single- or double-stranded polymer of deoxyribonucleotide or ribonucleotide bases and includes DNA and RNA molecules, both sense and anti-sense strands. The term comprehends cDNA, genomic DNA, recombinant DNA, and wholly or partially synthesized nucleic acid molecules. A polynucleotide may consist of an entire gene, or a portion thereof. A gene is a DNA sequence that codes for a functional protein or RNA molecule. Operable anti-sense polynucleotides may comprise a fragment of the corresponding polynucleotide, and the definition of “polynucleotide” therefore includes all operable anti-sense fragments. Anti-sense polynucleotides and techniques involving anti-sense polynucleotides are well known in the art and are described, for example, in Robinson-Benion et al., “Anti-sense techniques,” Methods in Enzymol. 254(23):363-375, 1995; and Kawasaki et al., Artific. Organs 20(8):836-848, 1996.

[0022] Identification of genomic DNA and heterologous species DNA can be accomplished by standard DNA/DNA hybridization techniques, under appropriately stringent conditions, using all or part of a polynucleotide sequence as a probe to screen an appropriate library. Alternatively, PCR techniques using oligonucleotide primers that are designed based on known genomic DNA, cDNA and protein sequences can be used to amplify and identify genomic and/or cDNA sequences. Synthetic polynucleotides corresponding to the identified sequences, and variants thereof, may be produced by conventional synthesis methods. All the polynucleotides provided by the present invention are isolated and purified, as those terms are commonly used in the art.

[0023] The polynucleotide sequences identified as SEQ ID NOS: 1-68 were derived from bovine mammary gland cells. Certain of the polynucleotides of the present invention may be “partial” sequences, in that they do not represent a full-length gene encoding a full-length polypeptide. Such partial sequences may be extended by analyzing and sequencing various DNA libraries using primers and/or probes and well known hybridization and/or PCR techniques. The sequences identified as SEQ ID NOS: 1-68 may thus be extended until an open reading frame encoding a polypeptide, a full-length polynucleotide and/or gene capable of expressing a polypeptide, or another useful portion of the genome is identified. Such extended sequences, including full-length polynucleotides and genes, are described as “corresponding to” a sequence identified as one of the sequences of SEQ ID NOS: 1-68, or a variant thereof, or a portion of one of the sequences of SEQ ID NOS: 1-68, or a variant thereof, when the extended polynucleotide comprises an identified sequence or its variant, or an identified contiguous portion (x-mer) of one of the sequences of SEQ ID NOS: 1-68 or a variant thereof.

[0024] The polynucleotides identified as SEQ ID NOS: 1-68 were isolated from bovine mammary gland cDNA libraries and represent sequences that are expressed in the tissue from which the cDNA was prepared. The sequence information may be used to isolate or synthesize expressible DNA molecules such as open reading frames or full-length genes, that then can be used as expressible or otherwise functional DNA in cows and other organisms. Similarly, RNA sequences, reverse sequences, complementary sequences, antisense sequences, and the like, corresponding to the polynucleotides of the present invention, may be routinely ascertained and obtained using the cDNA sequences identified as SEQ ID NOS: 1-68.

[0025] The polynucleotides identified as SEQ ID NOS: 1-68 contain open reading frames (“ORFs”) or partial open reading frames encoding polypeptides. Additionally, open reading frames encoding polypeptides may be identified in extended or full-length sequences corresponding to the sequences set out as SEQ ID NOS: 1-68. Open reading frames may be identified using techniques that are well known in the art. These techniques include, for example, analysis for the location of known start and stop codons, most likely reading frame identification based on codon frequencies, etc. Suitable tools and software for ORF analysis are available, for example, on the Internet. Additional tools and software for ORF analysis are available, for example, including GeneWise, available from The Sanger Center, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, United Kingdom; Diogenes, available from Computational Biology Centers, University of Minnesota, Academic Health Center, UMHG Box 43 Minneapolis Minn. 55455; and GRAIL, available from the Informatics Group, Oak Ridge National Laboratories, Oak Ridge, Tenn. Open reading frames and portions of open reading frames may be identified in the polynucleotides of the present invention. Once a partial open reading frame is identified, the polynucleotide may be extended in the area of the partial open reading frame using techniques that are well known in the art until the polynucleotide for the full open reading frame is identified. Thus, polynucleotides and open reading frames encoding polypeptides may be identified using the polynucleotides of the present invention.

[0026] Once open reading frames are identified in the polynucleotides of the present invention, the open reading frames may be isolated and/or synthesized. Expressible genetic constructs comprising the open reading frames and suitable promoters, initiators, terminators, etc., which are well known in the art, may then be constructed. Such genetic constructs may be introduced into a host cell to express the polypeptide encoded by the open reading frame. Suitable host cells may include various prokaryotic and eukaryotic cells, including mammalian cells. In vitro expression of polypeptides is also possible, as well known in the art.

[0027] Polypeptides encoded by the polynucleotides of the present invention may be expressed and used in various assays to determine their biological activity. Such polypeptides may be used to raise antibodies, to isolate corresponding interacting proteins or other compounds, and to quantitatively determine levels of interacting proteins or other compounds.

[0028] In another aspect, the present invention provides isolated polypeptides encoded, or partially encoded, by the above polynucleotides. As used herein, the term “polypeptide” encompasses amino acid chains of any length, including full-length proteins, wherein the amino acid residues are linked by covalent peptide bonds. The term “polypeptide encoded by a polynucleotide” as used herein, includes polypeptides encoded by a polynucleotide that comprises an isolated polynucleotide sequence or variant provided herein. Polypeptides of the present invention may be naturally purified products, or may be produced partially or wholly using recombinant techniques. Such polypeptides may be glycosylated with bacterial, fungal, mammalian or other eukaryotic carbohydrates or may be non-glycosylated. In specific embodiments, the inventive polypeptides comprise an amino acid sequence selected from the group consisting of SEQ ID NO: 69-136.

[0029] Polypeptides of the present invention may be produced recombinantly by inserting a polynucleotide sequence that encodes the polypeptide into a genetic construct and expressing the polypeptide in an appropriate host. Any of a variety of genetic constructs known to those of ordinary skill in the art may be employed. Expression may be achieved in any appropriate host cell that has been transformed or transfected with a genetic construct containing a polynucleotide that encodes a recombinant polypeptide. Suitable host cells include prokaryotes, yeast, and higher eukaryotic cells. Preferably, the host cells employed are Escherichia coli, insect, yeast, or a mammalian cell line such as COS or CHO. The polynucleotide sequences expressed in this manner may encode naturally occurring polypeptides, portions of naturally occurring polypeptides, or other variants thereof.

[0030] In a related aspect, polypeptides are provided that comprise at least a functional portion of a polypeptide having an amino acid sequence encoded by a polynucleotide of the present invention. As used herein, the “functional portion” of a polypeptide is that portion which contains the active site essential for affecting the function of the polypeptide, for example, the portion of the molecule that is capable of binding one or more reactants. The active site may be made up of separate portions present on one or more polypeptide chains and will generally exhibit high binding affinity.

[0031] Functional portions of a polypeptide may be identified by first preparing fragments of the polypeptide by either chemical or enzymatic digestion of the polypeptide, or by mutation analysis of the polynucleotide that encodes the polypeptide and subsequent expression of the resulting mutant polypeptides. The polypeptide fragments or mutant polypeptides are then tested to determine which portions retain biological activity, using, for example, the representative assays provided below.

[0032] Portions and other variants of the inventive polypeptides may also be generated by synthetic or recombinant means. Synthetic polypeptides having fewer than about 100 amino acids, and generally fewer than about 50 amino acids, may be generated using techniques well known to those of ordinary skill in the art. For example, such polypeptides may be synthesized using any of the commercially available solid-phase techniques, such as the Merrifield solid-phase synthesis method, where amino acids are sequentially added to a growing amino acid chain. See Merrifield, J. Am. Chem. Soc. 85:2149-2154, 1963. Equipment for automated synthesis of polypeptides is commercially available from suppliers such as Perkin Elmer/Applied BioSystems, Inc. (Foster City, Calif.), and may be operated according to the manufacturer's instructions. Variants of a native polypeptide may be prepared using standard mutagenesis techniques, such as oligonucleotide-directed, site-specific mutagenesis (Kunkel, Proc. Natl. Acad. Sci. USA 82:488-492, 1985). Sections of polynucleotide sequence may also be removed using standard techniques to permit preparation of truncated polypeptides.

[0033] In general, the polypeptides disclosed herein are prepared in an isolated, substantially pure, form. Preferably, the polypeptides are at least about 80% pure, more preferably at least about 90% pure, and most preferably at least about 99% pure. In certain embodiments, described in detail below, the isolated polypeptides are incorporated into pharmaceutical compositions or vaccines.

[0034] As used herein, the term “variant” comprehends nucleotide or amino acid sequences different from the specifically identified sequences, wherein one or more nucleotides or amino acid residues is deleted, substituted, or added. Variants may be naturally occurring allelic variants, or non-naturally occurring variants. Variant sequences (polynucleotide or polypeptide) preferably exhibit at least 75%, more preferably at least 90%, more preferably yet at least 95%, and most preferably, at least 98% identity to a sequence of the present invention. The percentage identity is determined by aligning the two sequences to be compared as described below, determining the number of identical residues in the aligned portion, dividing that number by the total number of residues in the inventive (queried) sequence, and multiplying the result by 100. By way of example only, assume a queried polynucleotide having 220 nucleic acids has a hit to a polynucleotide sequence in the EMBL database having 520 nucleic acids over a stretch of 23 nucleotides in the alignment produced by the BLASTN algorithm using the default parameters as described below. The 23 nucleotide hit includes 21 identical nucleotides, one gap and one different nucleotide. The percentage identity of the queried polynucleotide to the hit in the EMBL database is thus, 21/220 times 100, or 9.5%. The percentage identity of polypeptide sequences may be determined in a similar fashion.

[0035] Polynucleotide and polypeptide sequences may be aligned, and percentages of identical residues in a specified region may be determined against another polynucleotide or polypeptide, using computer algorithms that are publicly available. Two exemplary algorithms for aligning and identifying the similarity of polynucleotide sequences are the BLASTN and FASTA algorithms. Polynucleotides may also be analyzed using the BLASTX algorithm, which compares the six-frame conceptual translation products of a nucleotide query sequence (both strands) against a protein sequence database. The percentage identity of polypeptide sequences may be examined using the BLASTP algorithm. The BLASTN, BLASTP and BLASTX algorithms are available on the NCBI anonymous FTP server and from the National Center for Biotechnology Information (NCBI), National Library of Medicine, Building 38A, Room 8N805, Bethesda, Md. 20894, USA. The BLASTN algorithm Version 2.0.4 [Feb. 24, 1998], Version 2.0.6 [Sep. 16, 1998] and Version 2.0.11 [Jan. 20, 2000], set to the parameters described below, is preferred for use in the determination of polynucleotide variants according to the present invention. The BLASTP algorithm, set to the parameters described below, is preferred for use in the determination of polypeptide variants according to the present invention. The use of the BLAST family of algorithms, including BLASTN, BLASTP and BLASTX, is described at NCBI's website and in the publication of Altschul, et al., Nucleic Acids Res. 25: 3389-3402, 1997.

[0036] The FASTA and FASTX algorithms are available on the Internet and from the University of Virginia by contacting David Hudson, Vice Provost for Research, University of Virginia, P.O. Box 9025, Charlottesville, Va. 22906-9025, USA. The FASTA algorithm, set to the default parameters described in the documentation and distributed with the algorithm, may be used in the determination of polynucleotide variants. The readme files for FASTA and FASTX Version 1.0x that are distributed with the algorithms describe the use of the algorithms and describe the default parameters. The use of the FASTA and FASTX algorithms is described in Pearson and Lipman, Proc. Natl. Acad. Sci. USA 85:2444-2448, 1988; and Pearson, Methods in Enzymol. 183:63-98, 1990.

[0037] The following running parameters are preferred for determination of alignments and similarities using BLASTN that contribute to the E values and percentage identity for polynucleotides: Unix running command with the following default parameters: blastall-p blastn-d embldb-e 10-G 0-E 0-r 1-v 30-b 30-i queryseq-o results; and parameters are: -p Program Name [String]; -d Database [String]; -e Expectation value (E) [Real]; -G Cost to open a gap (zero invokes default behavior) [Integer]; -E Cost to extend a gap (zero invokes default behavior) [Integer]; -r Reward for a nucleotide match (blastn only) [Integer]; -v Number of one-line descriptions (V) [Integer]; -b Number of alignments to show (B) [Integer]; -i Query File [File In]; -o BLAST report Output File [File Out] Optional.

[0038] The following running parameters are preferred for determination of alignments and similarities using BLASTP that contribute to the E values and percentage identity of polypeptide sequences: blastall-p blastp-d swissprotdb-e 10-G 0-E 0-v 30-b 30-i queryseq-o results; the parameters are: -p Program Name [String]; -d Database [String]; -e Expectation value (E) [Real]; -G Cost to open a gap (zero invokes default behavior) [Integer]; -E Cost to extend a gap (zero invokes default behavior) [Integer]; -v Number of one-line descriptions (v) [Integer]; -b Number of alignments to show (b) [Integer]; -I Query File [File In]; -o BLAST report Output File [File Out] Optional.

[0039] The “hits” to one or more database sequences by a queried sequence produced by BLASTN, BLASTP, FASTA, or a similar algorithm, align and identify similar portions of sequences. The hits are arranged in order of the degree of similarity and the length of sequence overlap. Hits to a database sequence generally represent an overlap over only a fraction of the sequence length of the queried sequence.

[0040] The BLASTN, FASTA and BLASTP algorithms also produce “Expect” values for polynucleotide and polypeptide alignments. The Expect value (E) indicates the number of hits one can “expect” to see over a certain number of contiguous sequences by chance when searching a database of a certain size. The Expect value is used as a significance threshold for determining whether the hit to a database indicates true similarity. For example, an E value of 0.1 assigned to a polynucleotide hit is interpreted as meaning that in a database of the size of the EMBL database, one might expect to see 0.1 matches over the aligned portion of the sequence with a similar score simply by chance. By this criterion, the aligned and matched portions of the sequences then have a probability of 90% of being related. For sequences having an E value of 0.01 or less over aligned and matched portions, the probability of finding a match by chance in the EMBL database is 1% or less using the BLASTN algorithm. E values for polypeptide sequences may be determined in a similar fashion using various polypeptide databases, such as the SwissProt database.

[0041] According to one embodiment, “variant” polynucleotides and polypeptides, with reference to each of the polynucleotides and polypeptides of the present invention, preferably comprise sequences having the same number or fewer nucleic or amino acids than each of the polynucleotides or polypeptides of the present invention and producing an E value of 0.01 or less when compared to the polynucleotide or polypeptide of the present invention. That is, a variant polynucleotide or polypeptide is any sequence that has at least a 99% probability of being the same as the polynucleotide or polypeptide of the present invention, measured as having an E value of 0.01 or less using the BLASTN, FASTA or BLASTP algorithms set at the default parameters. According to a preferred embodiment, a variant polynucleotide is a sequence having the same number or fewer nucleic acids than a polynucleotide of the present invention that has at least a 99% probability of being the same as the polynucleotide of the present invention, measured as having an E value of 0.01 or less using the BLASTN algorithm set at the default parameters. Similarly, according to a preferred embodiment, a variant polypeptide is a sequence having the same number or fewer amino acids than a polypeptide of the present invention that has at least a 99% probability of being the same as the polypeptide of the present invention, measured as having an E value of 0.01 or less using the BLASTP algorithm set at the default parameters.

[0042] In addition to having a specified percentage identity to an inventive polynucleotide or polypeptide sequence, variant polynucleotides and polypeptides preferably have additional structure and/or functional features in common with the inventive polynucleotide or polypeptide. Polypeptides having a specified degree of identity to a polypeptide of the present invention share a high degree of similarity in their primary structure and have substantially similar functional properties. In addition to sharing a high degree of similarity in their primary structure to polynucleotides of the present invention, polynucleotides having a specified degree of identity to, or capable of hybridizing to an inventive polynucleotide preferably have at least one of the following features: (i) they contain an open reading frame or partial open reading frame encoding a polypeptide having substantially the same functional properties as the polypeptide encoded by the inventive polynucleotide; or (ii) they contain identifiable domains in common.

[0043] Alternatively, variant polynucleotides hybridize to a polynucleotide of the present invention under stringent conditions. As used herein, “stringent conditions” refers to prewashing in a solution of 6× SSC, 0.2% SDS; hybridizing at 65° C., 6× SSC, 0.2% SDS overnight; followed by two washes of 30 minutes each in 1× SSC, 0.1% SDS at 65° C. and two washes of 30 minutes each in 0.2× SSC, 0.1% SDS at 65° C.

[0044] The present invention also encompasses polynucleotides that differ from the disclosed sequences but that, as a consequence of the discrepancy of the genetic code, encode a polypeptide having similar enzymatic activity as a polypeptide encoded by a polynucleotide of the present invention. Thus, polynucleotides comprising sequences that differ from the polynucleotide sequences recited in SEQ ID NOS: 1-68 (or complements, reverse sequences, or reverse complements of those sequences) as a result of conservative substitutions are encompassed within the present invention. Additionally, polynucleotides comprising sequences that differ from the inventive polynucleotide sequences or complements, reverse complements, or reverse sequences as a result of deletions and/or insertions totaling less than 10% of the total sequence length are also contemplated by and encompassed within the present invention. Similarly, polypeptides comprising sequences that differ from the inventive polypeptide sequences as a result of amino acid substitutions, insertions, and/or deletions totaling less than 10% of the total sequence length are contemplated by and encompassed within the present invention, provided the variant polypeptide has similar activity to the inventive polypeptide.

[0045] The polynucleotides of the present invention may be isolated from various libraries, or may be synthesized using techniques that are well known in the art. The polynucleotides may be synthesized, for example, using automated oligonucleotide synthesizers (e.g., Beckman Oligo 1000M DNA Synthesizer) to obtain polynucleotide segments of up to 50 or more nucleic acids. A plurality of such polynucleotide segments may then be ligated using standard DNA manipulation techniques that are well known in the art of molecular biology. One conventional and exemplary polynucleotide synthesis technique involves synthesis of a single stranded polynucleotide segment having, for example, 80 nucleic acids, and hybridizing that segment to a synthesized complementary 85 nucleic acid segment to produce a 5 nucleotide overhang. The next segment may then be synthesized in a similar fashion, with a 5 nucleotide overhang on the opposite strand. The “sticky” ends ensure proper ligation when the two portions are hybridized. In this way, a complete polynucleotide of the present invention may be synthesized entirely in vitro.

[0046] As noted above, certain of the polynucleotides identified as SEQ ID NOS: 1-68 may be referred to as “partial” sequences, in that they may not represent the full coding portion of a gene encoding a naturally occurring polypeptide. Partial polynucleotide sequences disclosed herein may be employed to obtain the corresponding full-length genes for various species and organisms by, for example, screening DNA expression libraries using hybridization probes based on the polynucleotides of the present invention, or using PCR amplification with primers based upon the polynucleotides of the present invention. In this way one can, using methods well known in the art, extend a polynucleotide of the present invention upstream and downstream of the corresponding mRNA, as well as identify the corresponding genomic DNA, including the promoter and enhancer regions, of the complete gene. The present invention thus comprehends isolated polynucleotides comprising a sequence identified in SEQ ID NOS: 1-68, or a variant of one of the specified sequences, that encode a functional polypeptide, including full-length genes. Such extended polynucleotides may have a length of from about 50 to about 4,000 nucleic acids or base pairs, and preferably have a length of less than about 4,000 nucleic acids or base pairs, more preferably yet a length of less than about 3,000 nucleic acids or base pairs, more preferably yet a length of less than about 2,000 nucleic acids or base pairs. Under some circumstances, extended polynucleotides of the present invention may have a length of less than about 1,800 nucleic acids or base pairs, preferably less than about 1,600 nucleic acids or base pairs, more preferably less than about 1,400 nucleic acids or base pairs, more preferably yet less than about 1,200 nucleic acids or base pairs, and most preferably less than about 1,000 nucleic acids or base pairs.

[0047] As used herein, the term “x-mer,” with reference to a specific value of “x,” refers to a polynucleotide or polypeptide, respectively, comprising at least a specified number (“x”) of contiguous residues of: any of the polynucleotides provided in SEQ ID NOS: 1-68. The value of x may be from about 20 to about 600, depending upon the specific sequence.

[0048] Polynucleotides of the present invention comprehend polynucleotides comprising at least a specified number of contiguous residues (x-mers) of any of the polynucleotides identified as SEQ ID NOS: 1-68, or their variants. Polypeptides of the present invention comprehend polypeptides comprising at least a specified number of contiguous residues (x-mers) of any of the polypeptides corresponding to the polynucleotides of SEQ ID NOS: 1-68. According to preferred embodiments, the value of x is at least 20, more preferably at least 40, more preferably yet at least 60, and most preferably at least 80. Thus, polynucleotides of the present invention include polynucleotides comprising a 20 -mer, a 40 -mer, a 60 -mer, an 80 -mer, a 100 -mer, a 120 -mer, a 150 -mer, a 180 -mer, a 220 -mer, a 250 -mer, a 300 -mer, 400 -mer, 500 -mer or 600 -mer of a polynucleotide provided in SEQ ID NOS: 1-68, or a variant of one of the polynucleotides provided in SEQ ID NOS: 1-68. Similarly, polypeptides of the present invention include polypeptides comprising a 20 -mer, a 40 -mer, a 60 -mer, an 80 -mer, a 100 -mer, a 120 -mer, a 150 -mer, a 180 -mer, a 220 -mer, a 250 -mer, a 300 -mer, 400 -mer, 500 -mer or 600 -mer of an amino acid sequence provided in SEQ ID NO: 69-136 or a variant thereof.

[0049] The inventive polynucleotides may be isolated by high throughput sequencing of cDNA libraries prepared from bovine mammary gland tissue as described below in Example 1. Alternatively, oligonucleotide probes and/or primers based on the sequences provided in SEQ ID NOS: 1-68, can be synthesized and used to identify positive clones in either cDNA or genomic DNA libraries from bovine mammary gland cells by means of hybridization or polymerase chain reaction (PCR) techniques. Probes can be shorter than the sequences provided herein but should be at least about 10, preferably at least about 15 and most preferably at least about 20 nucleotides in length. Hybridization and PCR techniques suitable for use with such oligonucleotide probes are well known in the art (see, for example, Mullis et at., Cold Spring Harbor Symp. Quant. Biol., 51:263, 1987; Erlich, ed., PCR technology, Stockton Press: NY, 1989; and Sambrook et al., in Molecular cloning: a laboratory manual, 2nd ed., CSHL Press: Cold Spring Harbor, N.Y., 1989). Positive clones may be analyzed by restriction enzyme digestion, DNA sequencing or the like.

[0050] In addition, polynucleotide sequences of the present invention may be generated by synthetic means using techniques well known in the art. Equipment for automated synthesis of oligonucleotides is commercially available from suppliers such as Perkin Elmer/Applied Biosystems Division (Foster City, Calif.) and may be operated according to the manufacturer's instructions.

[0051] Oligonucleotide probes and primers complementary to and/or corresponding to SEQ ID NOS: 1-68, and variants of those sequences, are also comprehended by the present invention. Such oligonucleotide probes and primers are substantially complementary to the polynucleotide of interest. An oligonucleotide probe or primer is described as “corresponding to” a polynucleotide of the present invention, including one of the sequences set out as SEQ ID NOS: 1-68 or a variant thereof, if the oligonucleotide probe or primer, or its complement, is contained within one of the sequences set out as SEQ ID NOS: 1-68 or a variant of one of the specified sequences.

[0052] Two single stranded sequences are said to be substantially complementary when the nucleotides of one strand, optimally aligned and compared, with the appropriate nucleotide insertions and/or deletions, pair with at least 80%, preferably at least 90% to 95%, and more preferably at least 98% to 100%, of the nucleotides of the other strand. Alternatively, substantial complementarity exists when a first DNA strand will selectively hybridize to a second DNA strand under stringent hybridization conditions. Stringent hybridization conditions for determining complementarity include salt conditions of less than about 1 M, more usually less than about 500 mM, and preferably less than about 200 mM. Hybridization temperatures can be as low as 5° C., but are generally greater than about 22° C., more preferably greater than about 30° C., and most preferably greater than about 37° C. Longer DNA fragments may require higher hybridization temperatures for specific hybridization. Since the stringency of hybridization may be affected by other factors such as probe composition, presence of organic solvents, and extent of base mismatching, the combination of parameters is more important than the absolute measure of any one alone. DNA-DNA hybridization studies may be performed using either genomic DNA or DNA derived by preparing cDNA from the RNA present in the sample.

[0053] In addition to DNA-DNA hybridization, DNA-RNA or RNA-RNA hybridization assays are also possible. In the first case, the mRNA from expressed genes would then be detected instead of genomic DNA or cDNA derived from mRNA of the sample. In the second case, RNA probes could be used. In addition, artificial analogs of DNA hybridizing specifically to target sequences could also be used.

[0054] In specific embodiments, the inventive oligonucleotide probes and/or primers comprise at least about 6 contiguous residues, more preferably at least about 10 contiguous residues, and most preferably at least about 20 contiguous residues complementary to a polynucleotide sequence of the present invention. Probes and primers of the present invention may be from about 8 to 100 base pairs in length, or preferably from about 10 to 50 base pairs in length, or more preferably from about 15 to 40 base pairs in length. The probes can be easily selected using procedures well known in the art, taking into account DNA-DNA hybridization stringencies, annealing and melting temperatures, potential for formation of loops, and other factors which are well known in the art. Tools and software suitable for designing probes, and especially suitable for designing PCR primers, are available on the Internet, for example. In addition, a software program suitable for designing probes, and especially for designing PCR primers, is available from Premier Biosoft International, 3786 Corina Way, Palo Alto, Calif. 94303-4504. Preferred techniques for designing PCR primers are also disclosed in Dieffenbach and Dyksler, PCR Primer: a laboratory manual, CSHL Press: Cold Spring Harbor, N.Y., 1995.

[0055] A plurality of oligonucleotide probes or primers corresponding to a polynucleotide of the present invention may be provided in a kit form. Such kits generally comprise multiple DNA or oligonucleotide probes, each probe being specific for a polynucleotide sequence. Kits of the present invention may comprise one or more probes or primers corresponding to a polynucleotide of the present invention, including a polynucleotide sequence identified in SEQ ID NOS: 1-68.

[0056] In one embodiment useful for high-throughput assays, the oligonucleotide probe kits of the present invention comprise multiple probes in an array format, wherein each probe is immobilized in a predefined, spatially addressable location on the surface of a solid substrate. Array formats which may be usefully employed in the present invention are disclosed, for example, in U.S. Pat. Nos. 5,412,087, 5,545,531, and PCT Publication No. WO 95/00530, the disclosures of which are hereby incorporated by reference.

[0057] Oligonucleotide probes for use in the present invention may be constructed synthetically prior to immobilization on an array, using techniques well known in the art (See, for example, Gait, ed., Oligonucleotide synthesis a practical approach, IRL Press: Oxford, England, 1984). Automated equipment for the synthesis of oligonucleotides is available commercially from such companies as Perkin Elmer/Applied Biosystems Division (Foster City, Calif.) and may be operated according to the manufacturer's instructions. Alternatively, the probes may be constructed directly on the surface of the array using techniques taught, for example, in PCT Publication No. WO 95/00530.

[0058] The solid substrate and the surface thereof preferably form a rigid support and are generally formed from the same material. Examples of materials from which the solid substrate may be constructed include polymers, plastics, resins, membranes, polysaccharides, silica or silica-based materials, carbon, metals and inorganic glasses. Synthetically prepared probes may be immobilized on the surface of the solid substrate using techniques well known in the art, such as those disclosed in U.S. Pat. No. 5,412,087.

[0059] In one such technique, compounds having protected functional groups, such as thiols protected with photochemically removable protecting groups, are attached to the surface of the substrate. Selected regions of the surface are then irradiated with a light source, preferably a laser, to provide reactive thiol groups. This irradiation step is generally performed using a mask having apertures at predefined locations using photolithographic techniques well known in the art of semiconductors. The reactive thiol groups are then incubated with the oligonucleotide probe to be immobilized. The precise conditions for incubation, such as temperature, time and pH, depend on the specific probe and can be easily determined by one of skill in the art. The surface of the substrate is washed free of unbound probe and the irradiation step is repeated using a second mask having a different pattern of apertures. The surface is subsequently incubated with a second, different, probe. Each oligonucleotide probe is typically immobilized in a discrete area of less than about 1 mm². Preferably each discrete area is less than about 10,000 mm², more preferably less than about 100 mm². In this manner, a multitude of oligonucleotide probes may be immobilized at predefined locations on the array.

[0060] The resulting array may be employed to screen for differences in organisms or samples or products containing genetic material as follows. Genomic or cDNA libraries are prepared using techniques well known in the art. The resulting target DNA is then labeled with a suitable marker, such as a radiolabel, chromophore, fluorophore or chemiluminescent agent, using protocols well known for those skilled in the art. A solution of the labeled target DNA is contacted with the surface of the array and incubated for a suitable period of time.

[0061] The surface of the array is then washed free of unbound target DNA and the probes to which the target DNA hybridized are determined by identifying those regions of the array to which the markers are attached. When the marker is a radiolabel, such as ³²P, autoradiography is employed as the detection method. In one embodiment, the marker is a fluorophore, such as fluorescein, and the location of bound target DNA is determined by means of fluorescence spectroscopy. Automated equipment for use in fluorescence scanning of oligonucleotide probe arrays is available from Affymetrix, Inc. (Santa Clara, Calif.) and may be operated according to the manufacturer's instructions. Such equipment may be employed to determine the intensity of fluorescence at each predefined location on the array, thereby providing a measure of the amount of target DNA bound at each location. Such an assay would be able to indicate not only the absence and presence of the marker probe in the target, but also the quantitative amount as well.

[0062] In this manner, oligonucleotide probe kits of the present invention may be employed to examine the presence/absence (or relative amounts in case of mixtures) of polynucleotides in different samples or products containing different materials rapidly and in a cost-effective manner.

[0063] Another aspect of the present invention involves collections of a plurality of polynucleotide sequences of the present invention. A collection of a plurality of the polynucleotides of the present invention, particularly the polynucleotides identified as SEQ ID NOS: 1-68, may be recorded and/or stored on a storage medium and subsequently accessed for purposes of analysis, comparison, etc. Suitable storage media include magnetic media such as magnetic diskettes, magnetic tapes, CD-ROM storage media, optical storage media, and the like. Suitable storage media and methods for recording and storing information, as well as accessing information such as polynucleotide sequences recorded on such media, are well known in the art. The polynucleotide information stored on the storage medium is preferably computer-readable and may be used for analysis and comparison of the polynucleotide information.

[0064] Another aspect of the present invention thus involves storage medium on which are recorded a collection of the polynucleotides of the present invention, particularly a collection of the polynucleotides identified as SEQ ID NOS: 1-68. According to one embodiment, the storage medium includes a collection of at least 20, preferably at least 50, more preferably at least 100, and most preferably at least 200 of the polynucleotides of the present invention, preferably the polynucleotides identified as SEQ ID NOS: 1-68, including variants of those polynucleotides.

[0065] In another aspect, the present invention provides genetic constructs comprising, in the 5′-3′ direction, a gene promoter sequence; and an open reading frame coding for at least a functional portion of a polypeptide encoded by a polynucleotide of the present invention. In certain embodiments, the genetic constructs of the present invention also comprise a gene termination sequence. The open reading frame may be oriented in either a sense or antisense direction. Genetic constructs comprising a non-coding region of a gene coding for a polypeptide encoded by the above polynucleotides or a nucleotide sequence complementary to a non-coding region, together with a gene promoter sequence, are also provided. A terminator sequence may form part of this construct. Preferably, the gene promoter and termination sequences are functional in a host organism. More preferably, the gene promoter and termination sequences are common to those of the polynucleotide being introduced. The genetic construct may further include a marker for the identification of transformed cells.

[0066] Techniques for operatively linking the components of the genetic constructs are well known in the art and include the use of synthetic linkers containing one or more restriction endonuclease sites as described, for example, by Sambrook et al., in Molecular cloning: a laboratory manual, Cold Spring Harbor Laboratories Press: Cold Spring Harbor, N.Y., 1989. The genetic constructs of the present invention may be linked to a vector having at least one replication system, for example, E. coli, whereby after each manipulation, the resulting construct can be cloned and sequenced and the correctness of the manipulation determined.

[0067] Transgenic cells comprising the genetic constructs of the present invention are also provided by the present invention, together with organisms comprising such transgenic cells, products and progeny of such organisms. Techniques for stably incorporating genetic constructs into the genome of target organisms are well known in the art.

[0068] In one aspect, the present invention provides methods for using one or more of the inventive polypeptides or polynucleotides to treat disorders in a mammal, including a human. In this aspect, the polypeptide or polynucleotide is generally present within a pharmaceutical composition or immunogenic composition. Pharmaceutical compositions may comprise one or more polypeptides, each of which may contain one or more of the above sequences (or variants thereof), and a physiologically acceptable carrier. Immunogenic compositions may comprise one or more of the above polypeptides and an immunostimulant, such as an adjuvant, into which the polypeptide is incorporated.

[0069] Alternatively, a pharmaceutical or immunogenic composition of the present invention may contain a polynucleotide encoding one or more polypeptides as described above, such that the polypeptide is generated in situ. In such compositions, the polynucleotide may be present within any of a variety of delivery systems known to those of ordinary skill in the art, including nucleic acid expression systems, and bacterial and viral expression systems. Appropriate nucleic acid expression systems contain the necessary polynucleotide sequences for expression in a mammal (such as a suitable promoter and terminator signal). Bacterial delivery systems involve the administration of a bacterium (such as Bacillus Calmette-Guerin) that expresses an immunogenic portion of the polypeptide on its cell surface. In a preferred embodiment, the DNA may be introduced using a viral expression system (e.g., vaccinia or other poxvirus, retrovirus, or adenovirus), which may involve the use of a non-pathogenic, or defective, replication competent virus. Techniques for incorporating polynucleotides into such expression systems are well known in the art. The DNA may also be “naked,” as described, for example, in Ulmer et al., Science 259:1745-1749, 1993; and reviewed by Cohen, Science 259:1691-1692, 1993. The uptake of naked DNA may be increased by coating the DNA onto biodegradable beads, which are efficiently transported into the cells.

[0070] Routes and frequency of administration, as well as dosage, will vary from individual to individual. In general, the pharmaceutical compositions and vaccines may be administered by injection (e.g., intradermal, intramuscular, intravenous, or subcutaneous); intranasally (e.g., by aspiration); or orally. In general, the amount of polypeptide present in a dose (or produced in situ by the DNA in a dose) ranges from about 1 pg to about 100 mg per kg of host, typically from about 10 pg to about 1 mg per kg of host, and preferably from about 100 pg to about 1 pg per kg of host. Suitable dose sizes will vary with the size of the mammal, but will typically range from about 0.1 ml to about 5 ml.

[0071] While any suitable carrier known to those of ordinary skill in the art may be employed in the pharmaceutical compositions of this invention, the type of carrier will vary depending on the mode of administration. For parenteral administration, such as subcutaneous injection, the carrier preferably comprises water, saline, alcohol, a lipid, a wax, or a buffer. For oral administration, any of the above carriers or a solid carrier, such as mannitol, lactose, starch, magnesium stearate, sodium saccharine, talcum, cellulose, glucose, sucrose, and magnesium carbonate, may be employed. Biodegradable microspheres (e.g., polylactic galactide) may also be employed as carriers for the pharmaceutical compositions of this invention. Suitable biodegradable microspheres are disclosed, for example, in U.S. Pat. Nos. 4,897,268 and 5,075,109.

[0072] Any of a variety of immunostimulants may be employed in the immunogenic compositions of this invention to non-specifically enhance the immune response. Most adjuvants contain a substance designed to protect the antigen from rapid catabolism, such as aluminum hydroxide or mineral oil, and a non-specific stimulator of immune responses, such as lipid A, Bordetella pertussis, or Mycobacterium tuberculosis. Suitable adjuvants are commercially available as, for example, Freund's Incomplete Adjuvant and Freund's Complete Adjuvant (Difco Laboratories, Detroit, Mich.), and Merck Adjuvant 65 (Merck and Company, Inc., Rahway, N.J.). Other suitable adjuvants include alum, biodegradable microspheres, monophosphoryl lipid A, and Quil A.

[0073] The polypeptides of the present invention may additionally be used in assays to determine biological activity, to raise antibodies, to isolate corresponding ligands or receptors, in assays to quantitatively determine levels of protein or cognate corresponding ligand or receptor, as anti-inflammatory agents, and in compositions for mammary glands, connective tissue and/or nerve tissue growth or regeneration.

[0074] The polynucleotides of the present invention may be used for expression in a transgenic animal, as disclosed in U.S. Pat. No. 5,714,345, which teaches the use of transgenic animals capable of expressing a desired protein prepared by introducing into an egg or embryo cell of an animal, an expression construct containing the sequence corresponding at least in part to a specific polynucleotide, which encodes the desired protein. In the same manner, the desired protein corresponding to a selected polynucleotide sequence of the present invention, could be employed in transgenic animals for the production of milk containing the desired protein, as disclosed in U.S. Pat. No. 5,849,992.

[0075] In addition, the regulatory sequences contained in the present cDNA sequences, or regulatory sequences isolated by using the present sequences for genome screening and sequencing, as well known in the art, could be used in transgenic animals to direct the expression of a desired gene product according to the nature of the regulatory polynucleotide sequence, in a way similar to that taught in U.S. Pat. No. 5,850,000.

EXAMPLE 1

[0076] Isolation of cDNA Sequences from Bovine Mammary Gland cDNA Libraries

[0077] Bovine mammary gland cDNA expression libraries were constructed and screened as follows. mRNA was extracted from lactating bovine mammary tissue (Jersey breed, late lactating, non-pregnant cow, 2 hours post-milking) using standard protocols. mRNA was precipitated with ethanol and the total RNA preparate was purified using a Poly(A) Quik mRNA Isolation Kit (Stratagene, La Jolla, Calif.). A cDNA expression library was constructed from the purified mRNA by reverse transcriptase synthesis followed by insertion of the resulting cDNA clones in Lambda ZAP using a ZAP Express cDNA Synthesis Kit (Stratagene), according to the manufacturer's protocol. The resulting cDNAs were packaged using a Gigapack II Packaging Extract (Stratagene) employing 1 μl of sample DNA from the 5 μl ligation mix. Mass excision of the library was done using XL1-Blue MRF′ cells and XLOLR cells (Stratagene) with ExAssist helper phage (Stratagene). The excised phagemids were diluted with NZY broth (Gibco BRL, Gaithersburg, Md.) and plated out onto LB-kanamycin agar plates containing 5-bromo-4-chloro-3-indolyl-beta-D-galactoside (X-gal) and isopropylthio-beta-galactoside (IPTG).

[0078] Of the colonies plated and picked for DNA preparations, the large majority contained an insert suitable for sequencing. Positive colonies were cultured in NZY broth with kanamycin and cDNA was purified by means of REAL DNA minipreps (Qiagen, Venlo, The Netherlands). Agarose gel at 1% was used to screen sequencing templates for chromosomal contamination. Dye terminator sequences were prepared using a Biomek 2000 robot (Beckman Coulter Inc., Fullerton, Calif.) for liquid handling and DNA amplification using a 9700 PCR machine (Perkin Elmer/Applied Biosystems, Foster City, Calif.) according to the manufacturer's protocol.

[0079] The DNA sequences for positive clones were obtained using a Perkin Elmer/Applied Biosystems Division Prism 377 sequencer. cDNA clones were sequenced from the 5′ end. The sequences of the isolated polynucleotides are identified as SEQ ID NOS: 1-68, with the corresponding amino acid sequences being provided in SEQ ID NO: 69-136, respectively.

[0080] BLASTN Polynucleotide Analysis

[0081] The isolated cDNA sequences were compared to sequences in the EMBL DNA database using the computer algorithm BLASTN. Comparisons of DNA sequences provided in SEQ ID NOS: 1-68 to sequences in the EMBL DNA database (using BLASTN) were made as of August, 2000, using Version 2.0.11 [Jan. 20, 2000], and the following Unix runing command: blastall-p blastn-d embldb-e 10-GO-EO-r1-v 30-b 30-i queryseq o.

[0082] The sequences of SEQ ID NOS: 13, 21, 31, 37, 40, 57, 62-65, and 67 were determined to have less than 50% identity, determined as described above, to sequences in the EMBL database using the computer algorithm BLASTN, as described above. The sequences of SEQ ID NOS: 10, 15, 22, 25, 30, 48, 51 and 54 were determined to have less than 75% identity, determined as described above, to sequences in the EMBL database using the computer algorithm BLASTN, as described above. The sequences of SEQ ID NOS: 4-6, 8, 9, 12, 20, 29, 33, 35, 38, 39, 41-43, 47, 53, 60, 66 and 68 were determined to have less than 90% identity, determined as described above, to sequences in the EMBL database using the computer algorithm BLASTN, as described above. Finally, the sequences of SEQ ID NOS: 1, 7, 11, 14, 16, 18, 19, 23, 45, 46, 49, 50, 55, 56 and 61 were determined to have less than 98% identity, determined as described above, to sequences in the EMBL database using the computer algorithm BLASTN, as described above.

[0083] The sequences of SEQ ID NOS: 114, 125, 126, 132 and 135 were determined to have less than 50% identity, determined as described above, to sequences in the SwissProt database using the computer algorithm BLASTP, as described above. The sequences of SEQ ID NOS: 69, 72, 74, 89-92, 103, 116, 120, 122, 123, 127, 130 and 136 were determined to have less than 75% identity, determined as described above, to sequences in the SwissProt database using the computer algorithm BLASTP, as described above. The sequences of SEQ ID NOS: 71, 76, 78, 81, 83, 84, 86, 88, 94, 97, 101, 102, 104, 106, 107, 109, 110-112, 115, 118, 119, 131, 133 and 134 were determined to have less than 90% identity, determined as described above, to sequences in the SwissProt database using the computer algorithm BLASTP, as described above. Finally, the sequences of SEQ ID NOS: 70, 75, 77, 80, 85, 87, 93, 95, 98, 99, 105, 108 and 124 were determined to have less than 98% identity, determined as described above, to sequences in the SwissProt database using the computer algorithm BLASTP, as described above.

EXAMPLE 2

[0084] Expression of mRNA in Bovine Mammary Tissue

[0085] RNA was extracted from mammary gland tissue obtained from a non-pregnant heifer (Friesian Hereford cross, 2.5 years of age), a pregnant cow (Angus breed, 85 days pre-partum) and a lactating cow (Jersey breed, late lactating, non-pregnant and 2 hours post-milking), as well as from bovine liver, forebrain and kidney from an Angus Friesian cross heifer, using TRIzol (Gibco BRL, Gaithersburg, Md.) following the manufacturer's protocol. Sets of the various total RNA samples were run on 1.2% agarose/formaldehyde gels, 5 μg/lane. Following transfer to nitrocellulose membranes, RNA was cross-linked with ultraviolet light.

[0086] DNA probes were prepared from bacterial clones transformed with cDNA corresponding to SEQ ID NOS: 6 and 40 by excision of the insert of the cDNA clone using EcoRI and XhoI restriction endonucleases, or by PCR amplification of the insert of the cDNA clone using T7 and T3 primers (Gibco BRL), or by using the entire cDNA clone. Probes were radiolabeled with α-P³²-dATP using Rediprime DNA labeling kits (Amersham Pharmacia Biotech, Uppsala, Sweden). Blots were hybridized overnight with rotation at 65° C. in a buffer containing 10-20 ml of 500 mM NaH₂PO₄, 1 mM EDTA, 7% SDS and then washed for 15 minutes at 65° C., first in 2× SSC/0.1% SDS and then in 1× SSC/0.1% SDS. The blots were exposed to Kodak XAR X-ray film for appropriate times.

[0087] The insert of the cDNA clone corresponding to SEQ ID NO: 6 hybridized to two transcripts of approximately 3 kb and 1.1 kb. Transcripts were detected in all samples examined with the shorter transcript predominating.

[0088] The insert of the cDNA clone corresponding to SEQ ID NO: 40 hybridized strongly with a transcript of approximately 1.0 kb and less strongly with a transcript of approximately 2.0 kb in the lactating mammary gland sample. Lower levels of transcripts were detected in the mammary samples from a non-pregnant heifer and a pregnant non-lactating cow. No transcripts could be detected in the other tissue samples.

[0089] SEQ ID NOS: 1-136 are set out in the attached Sequence Listing. The codes for nucleotide sequences used in the attached Sequence Listing, including the symbol “n,” conform to WIPO Standard ST.25 (1998), Appendix 2, Table 1.

[0090] All references cited herein, including patent references and non-patent publications, are hereby incorporated by reference in their entireties.

[0091] While in the foregoing specification this invention has been described in relation to certain preferred embodiments, and many details have been set forth for purposes of illustration, it will be apparent to those skilled in the art that the invention is susceptible to additional embodiments and that certain of the details described herein may be varied considerably without departing from the basic principles of the invention.

0 SEQUENCE LISTING <160> NUMBER OF SEQ ID NOS: 136 <210> SEQ ID NO 1 <211> LENGTH: 271 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 1 gcaaaatgaa agtcctcacg tttgcctgca aggtacaaaa gaaggaccct aaggactggg 60 cagctcaata ccgaaaggca atggaagcag atatgaaggc tgcagctgag gctgcacttg 120 actccaaggc aagggctgac attagagctc agatgggcat tgggctcggc tctgagaatg 180 ctgctgggcc ctgcaactgg gatgaagctg atattggacc ctgggccaaa gcccgtatcc 240 aggcaggagc tgaagctaaa gccaaagccc a 271 <210> SEQ ID NO 2 <211> LENGTH: 431 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 2 atttgcaggt ccatctatgc tgtgtttgga gctgaaataa atctgaaagg aatccctgtg 60 tatagattta ttcttccatc ctttgctttt gcatctccat ttcaaaatcc agacaaccac 120 tgtttctgca cagaaaaaat catctcaaaa aattgtacct tatatggtgt gctagacatt 180 ggcaaatgca aagaaggaaa acctgtgtac atttcacttc ctcattttct acatggaagt 240 cctgaacttg cagaacctat tgaaagctta agtccaaatg aagaagaaca tagcacgtac 300 ttagatgttg aacctataac tggatttact ttacggtttg caaaacggct gcaggtcaac 360 atgctggtca agccagcaaa aaaaattgaa gcattgaaga atctgaagca caactatatt 420 gtccctattc t 431 <210> SEQ ID NO 3 <211> LENGTH: 247 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 3 tcgggactta ggaaaacgta tccaggaccc aagaggaatg tatcggtgtg gtgaaaacac 60 ccaacaactt attctgcaag tatactatcg aatgtgccag aactgtgtgg agctggacac 120 agccaccctg gcaggcatga tcatcaccga catcattgcc actgtgctcc ttgctttggg 180 tgtctactgc tttgctggac atgagactgg aagattctcc agggctgctg acactcaagc 240 tctgatg 247 <210> SEQ ID NO 4 <211> LENGTH: 340 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 4 ctgccgctgc caacctggat attacgggga tggatttcag tgcacacctg agcccaccca 60 gaggccccgg accgtctgtg agcgctggag ggaaagcctg ctggagcact acgggggcac 120 ccccagggac gaccagtatg tgcctcagtg cgacgacctg ggccacttca ccccgctgca 180 gtgccatggc aagagtgact tctgctggtg tgtcgaccag gacggcagag aggtgcaggg 240 cacccgctcg cagccaggca tcacccctgc atgtataccc accgtggctc cacccacggt 300 ccggcccaca ccccggcccg acgtgacccc tccaccagtg 340 <210> SEQ ID NO 5 <211> LENGTH: 401 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 5 caacactttt ctttctcccg ccctaacggt cgccgcggcc aactgcctcg cccgcctggc 60 cgcctacccc gccttctctt ctgtgcggct accgcgcggc cctgtgtccc tctcgcccgg 120 cggtatccgc ttgccgctgc caccgccgcc tcgtcttgct gtccggccag ctggcccgcc 180 ccgctgcagt gatgtgcgac aaggaattca tgtgggccct gaaaaacgga gacctagatg 240 aggtgaaaga ctatgtggcc aagggagaag atgtcaaccg gacactagaa ggtggaagaa 300 agcctcttca ttatgcagca gattgtggac agcttgaaat cctggaattt ctgctgctga 360 aaggagcaga tatcaatgct ccagataaac atcatatcac a 401 <210> SEQ ID NO 6 <211> LENGTH: 873 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 6 cggaggctgt gtcccacaga cactagcatc atgaatatat ttgatcggaa gatcaacttt 60 gatgcactct ttaaattttc ccacataacc ccctcgacac agcagcacct gaagaaggtt 120 tatgccagtt ttgccctctg tatgtttgtg gcggctgcgg gggcctatat ccatgtggtc 180 acccatttca ttcaggctgg cctgctctct gccttgggct ctttggggtt gatgatttgg 240 ctgatggcaa cacctcacag ccatgaaact gagcaaaaaa gactgggact tctggctgga 300 tttgctttcc ttacaggagt tggcctgggc cctgctctgg acttgtgcat tgccatcaac 60 cccagcatcc ttcccactgc cttcatgggc acagcaatga tcttcacctg cttcaccctg 420 agtgcactct atgccaggcg ccgtagctac ctctttctag gaggtatctt gatgtcggcc 480 atgagcctca tgctcttgtc ttccctgggg aaccttttct tcggatctgt ttggcttttc 540 caggcaaacc tgtatatggg gctggtggtc atgtgtggct ttgtcctttt tgatactcaa 600 ctcattattg aaaaggctga aaatggagat aaagattata tctggcactg cgttgacctc 60 ttcttggatt tcgtaactct cttcagaaag ctcatgatga tcctggctat gaatgagaag 720 gataagaaga agaagaagtg aagcagccat ccagccttgc ccaatttgac ttcctctccc 780 tccgcccttc atttcctctt tgcacacatt acaggtggcg tggtctgtga taatgaaaag 840 catcagaaaa gctttaaaaa aaaaaaaaaa aaa 873 <210> SEQ ID NO 7 <211> LENGTH: 486 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 7 agtgcacgtg tctggacggg tcggtgggct gcgtgcccct atgcagcgtg gacgtccgcc 60 tgcccagccc cgactgcccc ttccctcgga gggtcaaact gcccgggaaa tgctgcgagg 120 aatgggtgtg tgatgagccc aaggagcaca ccgtggtcgg ccctgcgctc gcagcttacc 180 ggccggaaga cacgtttggc ccagacccaa ccatgatccg agccaactgc ctggtccaga 240 ccacagagtg gagtgcctgt tccaagacct gcggaatggg catctccacc cgggttacca 300 atgacaacgc attctgcagg ctggagaagc agagccgcct ctgcatggtc aggccttgcg 60 aagctgacct ggaggagaac attaagaaag gcaaaaagtg catccggacc cccaaaatct 420 ccaagcctat caagtttgag ctttctggct gcaccagcat gaagacatac cgagctaaat 480 tctgcg 486 <210> SEQ ID NO 8 <211> LENGTH: 362 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 8 ttgccttgaa gaaagtgaaa ttccaagcca aactagaaca tgaatacatc cagaacttca 60 aaatactaca agcaggtttt aagaggatgg gtgttgacaa aataattcct gtggacaaat 120 tagtaaaagg aaagtttcag gacaattttg aatttgttca gtggttcaag aagttttttg 180 atgcaaacta tgatggaaaa gagtatgacc ctgtggctgc cagacaaggt caagaaactg 240 caatggcccc ctcccttgtt gctcccgctc tgaacaaacc gaagaaacct ctcagctcta 300 gcagtgcagc tccacagagg cccattacaa cacacagaac tactgcaacc cctaaagctg 360 gc 362 <210> SEQ ID NO 9 <211> LENGTH: 435 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 9 tgaagactca caagaaccct gccttgaagg ctcagagtgg tctgatacga agtggcccca 60 aacccttctc tgcatctaaa ccagatcccc ccaaaccagt cgcaaagaag gagccagccc 120 tacttgaact ggagggcaag aagtggagag tggaaaatca ggagaatgtt tccaacctga 180 tgatagagga tacagagctg aaacaggtgg cttacatatt caagtgtgtg aactcaacat 240 tgcagatcaa gggcaaaatt aactccatta ctgtagataa ctgtaagaaa cttggtctgg 300 tgtttgatga cgtggtgggc attgtggaga taatcaatag taaggatgtc aaagttcagg 360 taatgggtaa agtgccaacc atttccatca acaaaacaga tggctgccac gtttacctga 420 gcaagaactc cctgg 435 <210> SEQ ID NO 10 <211> LENGTH: 301 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 10 ggaaagacgg agggtggccc agcagaagca gcagcagttg gagcaggagc agttccatgc 60 cttcgaggag atgatccgga accaggagct agaaaaggaa cgactgaaga ttgtgcagga 120 gtttgggaag gtggaccctg tcctgggggg cccactggtg cctgacttgg agacgccctc 180 cctagatgtg ttccccacgg tgcctgctat acccacacag ccttcagact gtaatgcagc 240 tgtgaggctt gccaagccac cggtggtgga cagatccttg aaacctggag cactgaacaa 300 c 301 <210> SEQ ID NO 11 <211> LENGTH: 410 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 11 gatattttaa gggtataatg caagatgtgc aattacttgt catgccccaa ggatttattg 60 ctcagtgccc agatcttaat cgcacctgtc caacatgcaa tgactttcac ggactcgtgc 120 agaaaatcat ggaactgcag gacattttag ccaaaacatc agccaagctg tctcgagccg 180 agcagcgaat gaatagactg gaccagtgct actgtgagag gacttgcacc atgaagggaa 240 ccacctaccg agaattcgag tcatggacag acggctgcaa gaactgcaca tgcctgaatg 300 gaaccatcca gtgtgaaact ctgatttgcc caaatcctga ctgccccctc aagtcggctc 360 ccgcatacgt ggatggcaag tgctgtaagg aatgcaaatc catatgccag 410 <210> SEQ ID NO 12 <211> LENGTH: 381 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 12 cgggtgcccg gccgccacgg ctacgccgcc gagttctccc cgtacctgcc gggccgactg 60 gcctgcgccg cctcgcagca ctacggcatc gcgggcagtg gaactctgct aatattggat 120 caaaatgaat ctgggcttag gctttttaga agctttgact ggaatgacgg tttgtttgac 180 gtgacctgga gtgagaacaa tgagcatgtg ctggtcacct gcagtggcga cggctcctta 240 cagctctggg ataccgccag ggccacaggg ccgctgcagg tcttcaagga gcacactcag 300 gaggtgtaca gtgttgattg gagccaaacc agaggtgaac agcttgtggt gtctggctca 360 tgggatcaaa ctgtcaaact g 381 <210> SEQ ID NO 13 <211> LENGTH: 454 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 13 ctcaggcctc agatggcctc ttccaaaaac tatggctctc cactcatcag tggttccact 60 ccaaagcatg agcgtggctc tcccagccat agtaagtcac cagcatatac cccccagaat 120 ctggacagtg aaagtgagtc aggctcctcc atagcagaga aatcttatca gaacagtcct 180 agctcagatg atggcatccg acctcttcca gaatacagca cagagaagca taagaagcac 240 aaaaaagaaa agaagaaagt aaaggacaaa gatagggacc gggacaaaga ccgagacaag 300 aaaaaatctc atagcatcaa gccagagagt tggtctaaat cacccatctc ttcagaccag 360 tccttgtcta tgacaagtaa cacaatctta tctacagaca ggccctcaag gctcagccct 420 gactttatga ttggggagga agatgacgat ctta 454 <210> SEQ ID NO 14 <211> LENGTH: 481 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 14 tctggaagaa gaatacaccg tttctgtatg acctggttat gacccatgct cttcagtggc 60 cgagtcttac cgttcagtgg cttcctgaag tgactaaacc ggaaggaaag gattatgccc 120 ttcattggct agggctgggg actcacacat ctgatgagca gaatcatctc gtggttgctc 180 gagtccatat tccgaatgat gatgcacagt ttgatgcttc ccactgtgac agtgaaaagg 240 gtgaatttgg tggctttggt tctgtaacag gaaaaattga atgtgaaatt aaaattaacc 300 atgaaggaga agtaaaccgt gctcgttaca tgccgcagaa tcctcacatc attgctacaa 360 aaacaccatc ttctgatgtg ctggtttttg actatacgaa gcaccctgct aaaccagacc 420 caagtggaga gtgtaatcct gaccttaggc taagaggcca ccaaaaggaa ggctatggcc 480 t 481 <210> SEQ ID NO 15 <211> LENGTH: 458 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 15 ctcccacgaa catcccagca ctcaagacca gggtaatcat cttgctgaag agtgtttatc 60 ttcagatgaa gggactcccc caagcattaa aaaaatcata catgtgctgg agaaggtcca 120 gtatcttgag caagaagtag aagagttcgt aggaaaaaag acagacaaag cctactggct 180 tctggaagag atgctaacca aggaacttct ggaactggat tcagttgaaa ctgggggcca 240 ggactccgtc cggcaggcca ggaaagaggc ggtttgtaaa atccaggcca tactggaaaa 300 attggaaaaa aagggattat gaagggattt agaacaaagg ggaagcctgt tactaactcg 360 accaaagaac tcttgatttt ggttaattac cctctttttg aaatgcctgt tgacgacaag 420 aagcaataca ttccaacttt cctttgatag aaagcttg 458 <210> SEQ ID NO 16 <211> LENGTH: 408 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 16 cgcagagcgg cggtgcaccc acaggccccg agatgcaggc cctcgtgcta ctcctctgga 60 ctggagccct gcttgggttt ggccgctgcc agaacgccgg ccaggaggcg ggctctctga 120 cccctgagag cacgggggca ccagtggagg aagaggatcc cttcttcaag gtccctgtga 180 acaagctggc ggcagccgtc tccaacttcg gctacgacct gtaccgcgtg agatccggtg 240 agagccccac cgccaatgtg ctgctgtctc cgctcagcgt ggccacggcg ctctctgccc 300 tgtcgctggg tgcggaacag cggacagaat ccaacattca ccgggctctg tactacgacc 360 tgatcagtaa cccagacatc cacggcacct acaaggacct ccttgcct 408 <210> SEQ ID NO 17 <211> LENGTH: 459 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 17 tcttgcggcg cgtgagcccg aggcagccat tgcccgcttg gtgttctcta gtacctgtga 60 ttcttatcct taaagatgcc tgaggaagtg caccatggag aggaggaggt ggagacattt 120 gccttccagg cagaaattgc ccaactcatg tctcttatta tcaacacctt ctattccaac 180 aaggaaattt ttcttcggga gttgatcagt aatgcttctg atgccttaga caagattcgc 240 tatgagagcc tgacagaccc ttccaaattg gacagtggta aagagctgaa aattgacatc 300 atcccaaacc cccaggagcg tactctgact ctggtagaca caggcattgg catgaccaaa 360 gctgatcttg taaataattt gggaaccatt gccaagtctg gcactaaagc gtttatggag 420 gctcttcagg ctggtgcaga catctccatg attgggcaa 459 <210> SEQ ID NO 18 <211> LENGTH: 354 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 18 cgcaagaaac gcaaaatccg ggaggagatt gagcactttg gaatcaaggt ctaccagttc 60 ccagactgtg actctgatga ggatgaggac ttcaaatcac aggacctggc cctaaaggaa 120 agcatcccat ttgctgtcat tggcagtaac actgtggtag aggccagagg gcgtcgagtt 180 cggggccggc tctacccctg gggcatcgtg gaagtggaaa acccagggca ctgcgacttt 240 gtgaagctga ggacaatgct ggtgcgtact cacatgcagg acctgaagga cgtgacgcgg 300 gagacacatt atgagaacta ccgggcacag tgcatccaga gcatgacccg cctg 354 <210> SEQ ID NO 19 <211> LENGTH: 339 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 19 cgaggacctg cggaacaaga tccacacggc caccgtggac aatgccaacc tcctgcttca 60 gatcgacaat gcccgcctgg ctgctgatga cttccgcacc aagtttgaga cagagcaggc 120 cctgcgtgtg agcgtggagg ccgacatcaa cggcctgcgc agggtgctgg acgagctgac 180 cctggccaga gccgacctgg agatgcagat cgagaacctc aaggaggagc tggcctacct 240 ccgcaagaat cacgaggagg agatgaaagc cctgcgaggc caggtgggcg gcgagatcaa 300 cgtggagatg gacgctgccc ccggcgtgga cctgagccg 339 <210> SEQ ID NO 20 <211> LENGTH: 653 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 20 ataagtatga agatgaaatt aaccatcgca cagctgctga gaatgagttt gtggtgttga 60 agaaggatgt ggatgttgcc tacatgaaca aggtggagtt ggaggccaag gtggataccc 120 tgaatgatga gatcaacttc ctcaggaccc tctatgagca ggagctgaaa gagctgcagt 180 ctgaggtctc agacacatcc gtggtcctgt ccatggacaa caaccgctcc ctggacttgg 240 acagcatcat tgctgaagtc aaggcccagt atgaggagat cgccaaccgc agccgggcgg 300 aggccgaggc ctgttaccag accaagtttg agaccctcca ggcccaggct gggaagcacg 60 gggacgacct ccggaatacc cggaatgaga ttgcggacat gaaccgggct gtccagaggc 420 tgcaggccga gatcgacagc gtcaagaacc agcgctccaa gttggaagcc gccattgccg 480 atgctgaaca gcgtggggaa ctggctgtca aggatgcacg ggccaagcag gaggatctgg 540 aggccgccct gcagaaggcc aagcaggaca tgacccggca gctgcgggag taccaggagc 600 tcatgaacgt caagctggcc ctggacattg agatcgccac ctaccgcaag ctg 653 <210> SEQ ID NO 21 <211> LENGTH: 430 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 21 gaaccttcca gctggacggt gagcacgatg gtgcctgtcc tgctggccct gctgctactt 60 ctgggccctg cagtctccga ggagacccag gctgggaatt actctctaag cttcctctac 120 accgggctgt ccaagccccg tgagggcttc cccagcttcc aggccgttgc ctacctcaat 180 gaccagccct tcttccacta caatagtgaa ggcaggaggg ccgagcccct ggcgccatgg 240 agtcaggtgg aaggaatgga ggactgggag aaggagagtg cccttcagag ggccagagag 300 gacatcttca tggagaccct gagcgatatc atggactact acaaggacag agaagggtct 360 cacacctttc aaggagcatt cggctgtgag ctccggaata acgaaagtag tggagcattc 420 tgggggtacg 430 <210> SEQ ID NO 22 <211> LENGTH: 525 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 22 ttttcggcag cgggaccaca ctgaccgtcc tgggtcagcc caagtccgca ccctcggtca 60 ccctgttccc gccctccaag gaggagctcg acaccaacaa ggccaccctg gtgtgtctca 120 tcagcgactt ctacccgggt agcgtgaccg tggtctggaa ggcagacggc agcaccatca 180 cccgcgacgt gaagaccacc cggccctcca aacagagcaa cagcaagtac gcggccagca 240 gctacctgag cctgacagac agcgactgga aatcgaaagg cagttacagc tgcgaggtca 300 cgcacgacgg gagcaccgtg acgaagacag tgaagccctc agagtgtcct tagggcctg 360 gacccccacc ctcgggggcc ctctggccca caccccctcc cccacctctc catggaccc 420 tgagccccta cccaggtcgc ctcacaccag gggcctctcc tccctccctg ttcctgctc 480 tcctgaataa agaccttctc atttatcagc aaaaaaaaaa aaaaa 525 <210> SEQ ID NO 23 <211> LENGTH: 374 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 23 cgacgtggag gtgcacacgg ccaggacgaa gccgagagag gagcagttca acagcaccta 60 ccgcgtggtc agcgccctgc gcatccagca ccaggactgg ctgcagggaa aggagttcaa 120 gtgcaaggtc aacaacaaag gcctcccggc ccccattgtg aggaccatct ccaggaccaa 180 agggcaggcc cgggagccgc aggtgtatgt cctggcccca ccccgggaag agctcagcaa 240 aagcacgctc agcctcacct gcctgatcac cggtttctac ccagaagaga tagacgtgga 300 gtggcagaga aatgggcagc ctgagtcgga ggacaagtac cacacgaccg caccccagct 360 ggatgctgac ggct 374 <210> SEQ ID NO 24 <211> LENGTH: 627 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 24 ccgaaaccca aggacaccct cacaatctcg ggaacgcccg aggtcacgtg tgtggtggtg 60 gacgtgggcc acgatgaccc cgaggtgaag ttctcctggt tcgtggacaa cgtggaggta 120 aacacagcca cgacgaagcc gagagaggag cagttcaaca gcacctaccg cgtggtcagc 180 gccctgcgca tccagcacca ggactggact ggaggaaagg agttcacgtg caaggtccac 240 aacgaaggcc tcccggcccc catcgtgagg accatctcca ggaccaaagg gcaggcccgg 300 gagccgcagg tgtatgtcct ggccccaccc caggaagagc tcagcaaaag cacggtcagc 360 ctcacctgca tggtcaccag cttctaccca gactacatcg ccgtggagtg gcagagaaat 420 gggcagcctg agtcggagga caagtacggc acgaccccgc cccagctgga cgccgacagc 480 tcctacttcc tgtacagcaa gctcagggtg gacaggaaca gctggcagga aggagacacc 540 tacacgtgtg tggtgatgca cgaggccctg cacaatcact acacgcagaa gtccacctct 600 aagtctgcgg gtaaatgagc ctcacgt 627 <210> SEQ ID NO 25 <211> LENGTH: 433 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 25 ctggcgtcgg cgccctaccc aaagtccagg gaaggagcct ggccgggacg cgcgcaccat 60 gccctacctg ctcatcagca cccagatacg catggaggtg ggccccaccg tggtgggcga 120 tgagcactca gatccagaac tgatgcagca tctgggggcc tcaaaaagaa gtgtcctggg 180 aaacaacttc tctgagtact acgtgaatga ccctcctcga atcgtcctgg acaagctgga 240 gcgcaggggc ttccgtgtgc tgagcatgac aggggtgggc cagacgctgg tgtggtgcct 300 gcacaaggag tgaccctccc acacggagga gcgccagtca cacttctttg gagtggctgc 360 catgggcccc gaccccaaga ccctgccttg ctcaccaccc tgccccttct tcccaaatca 420 tccttctcct tgg 433 <210> SEQ ID NO 26 <211> LENGTH: 725 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 26 tgaaagacaa gaagtcgtgc cacaccgccg tggacaggac tgcaggctgg aacatcccca 60 tgggcctgat cgtaaccaga caggctcctg cgcatttgat gaattcttta gtcagagctg 120 tgcccctggg gctgacccga aatccagact ctgtgccttg tgtgctggcg atgaccaggg 180 cctggacaag tgtgtgccca actctaagga gaagtactat ggctataccg gggctttcag 240 gtgcctggct gaggacgttg gggacgttgc ctttgtgaaa aacgacacag tctgggagaa 300 cacgaatgga gagagcactg cagactgggc taagaacttg aatcgtgagg acttcaggtt 360 gctctgcctc gatggcacca ggaagcctgt gacggaggct cagagctgcc acctggcggt 420 ggccccgaat cacgctgtgg tgtctcggag cgatagggca gcacacgtga aacaggtgct 80 gctccaccag caggctctgt ttgggaaaaa tggaaaaaac tgcccggaca agttttgttt 540 gttcaaatct gaaaccaaaa accttctgtt caatgacaac actgagtgtc tggccaaact 600 tggaggcaga ccaacgtatg aagatatttg gggacagagt atgtcacggc cattgccaac 660 ctgaaaaaat gctcaacctc cccgcttctg gaagcctgcg ccttcctgac gaggtaaagc 720 ctgca 725 <210> SEQ ID NO 27 <211> LENGTH: 745 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 27 cccggccctg gcccgggccc ggggagcaac ttgacttcgg ccccagggcc ctccaccaca 60 acacgctcgc tgaccgcatg ccctgaggag tccccgctgc tcgtcggccc catgctgatt 120 gagtttaaca tacctgtgga cctgaagctt gtggagcacc agaacccgaa ggtgaagttg 180 ggtggtcgct acacccccac ggactgcatc tctcctcaca aggtggccat catcattcca 240 ttccgcaacc ggcaggaaca cctcaagtac tggctgtatt acttgcaccc aatcctacag 300 cgtcagcagt tagactatgg catctatgtt atcaaccagg ctggagagtc catgttcaac 360 cgcgcaaagc tcctcaatgt tggctttaaa gaggccttga aggactatga ctacaactgc 420 tttgtgttta gcgatgtgga cctcatccca atgaacgacc ataacaccta caggtgcttt 80 tcacagccac ggcacatttc tgtagcaatg gataagtttg gatttagcct accttacgtg 540 cagtattttg gaggtgtctc tgctctaagt aaacaacagt ttctcagcat caatggattt 600 cctaataact actggggctg gggaggtgaa gatgatgaca tttataagca gattagcttt 660 agaggcatgt ctgtgtctcg cccaaatgct gtgatcggga agtgtcggat gatccgcact 720 cgagagacaa agaaaaatga accta 745 <210> SEQ ID NO 28 <211> LENGTH: 476 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 28 gaagtatcgg aatccagaaa ccagtagggc atgtggacat ttaccctaac ggaggcactt 60 tccaaccagg atgtaacatt ggggaagctc tccgtgtgat tgcagagaga ggccttggag 120 atgtggatca gctggtgaag tgctcccacg aacgttccgt tcatctcttc attgactctc 180 tgttgaatga agaaaatcca agtaaggcct accggtgcaa ttccaaagaa gcctttgaga 240 aaggtctctg cctgagctgc agaaagaacc gttgcaacaa catgggctac gagatcaaca 300 aggtcagagc caaaagaagc agcaagatgt acctgaagac tcgttctcag atgccttaca 360 aagtcttcca ttaccaagta aagatacatt tttctggaac tgagagtaat acatacacca 420 accaggcctt cgagatctct ctgtatggca ctgtggctga gagcgagaac atccct 476 <210> SEQ ID NO 29 <211> LENGTH: 452 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 29 cgctgctgta gccatggccc cgattaaggt tggagatgcc attccatcgg tggaggtatt 60 tgaaaaggag ccgggcaaca aggtgaacct ggcagagctg ttcaaaggca agaagggagt 120 gctgtttggc ctccctgggg cctttacccc tggtggttcc aagacccacc tgccagggtt 180 cgtggagcag gctgatgctc tgaaggccaa ggggatccag gtggtggcat gtctgaccgt 240 taatgatgtc tttgtaactg aagagtgggc acgcgcccac aaggcagagg gcaaggttcg 300 gctcctggca gaccccagtg ggacttttgg gaaggagaca gatttgttac ttgatgattc 360 actgctcttt ctctttggga atcaccgact gaagaggttc tccatggtga tagaggatgg 420 catcgtcaaa tccctgaacg tggagccaga tg 452 <210> SEQ ID NO 30 <211> LENGTH: 434 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 30 ctggagccag ctaagctcag cggagcagat ataaaccgag aagggcaaac tcatcgagag 60 ggcgtcttcg ggaccatggc gaatggatat acatatgaag attatcaaga cactgcaaaa 120 tggcttttgt ctcataccga acagcgacct caagtggcag tgatctgtgg ttctgggtta 180 ggaggtctgg ttaacaaatt gactcaagcc cagacctttg actacagtga aataccaaac 240 tttccagaaa gtacagtgcc aggtcatgct ggtcgactgg tgtttgggat cttgaatggc 300 agagcctgtg tgatgatgca gggcaggttc cacatgtatg aaggctatcc gttttggaag 360 gtgacattcc cagtgagggt tttccggctt ctgggtgtgg agaccctagt ggtcaccacg 420 cagctgaggg ctca 434 <210> SEQ ID NO 31 <211> LENGTH: 406 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 31 tatcggcgag ggtgaagatt tgatcaagtg gaaggcactg tttgaggagg tccctgagtt 60 gttaaccgag acagaaaaaa aggaatggat tgacaaactt aatgaagttt ccatcagctc 120 tgatgccttc tttcctttcc gggacaatgt agacagagca aaaggagtgg cgtggcctac 180 atcgctgccc cttccggttc tgccgctgac aaagttgtga tcgaggcttg cgatgagctg 240 ggaataatcc ttgctcatac gaatctccgg ctcttccatc actgacttca tcaatacatt 300 attttatacc ctgcctctgt gtaggtgaaa aatcacatac ggaattttga aaatggcctt 360 tgtttaaaac taaagcataa aatctaataa tcttcagtct atactg 406 <210> SEQ ID NO 32 <211> LENGTH: 428 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 32 cttccccgac tccaggatgc ctccctacac catcgtctac ttcccggttc aagggcgctg 60 cgaggccatg cgcatgctgc tggccgacca gggccagagc tggaaggagg aggtcgtagc 120 catgcagagc tggctgcagg gcccactcaa ggcctcctgc ctgtacgggc agctccccaa 180 gttccaggac ggagacctca cgctgtacca gtccaatgcc atcctgcggc acctgggccg 240 caccctcggg ctgtatggga aggaccagca ggaggcggcc ctggtggaca tggtgaatga 300 cggtgtagag gaccttcgct gcaaatacgt ctccctcatt tacaccaact acgaggcggg 360 caaggaggac tatgtgaagg cgctgcccca gcacctgaag cctttcgaga ccctgctgtc 420 ccagaaca 428 <210> SEQ ID NO 33 <211> LENGTH: 305 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 33 cattcagcga gctcaccaga acacgtggga agtgtaccct cccttcttat tttttctagc 60 tgtcggaggt gtttaccacc cacgtatagt ttctggcttg ggcttggcct ggatcgttgg 120 acgagtcctt tatgcttacg gctattacac aggagaaccc agaaagcggc agcggggagc 180 cctgagcttc atcgccctca ttggcctgat gggcaccact gtgtgctctg ccttccagca 240 tcttggttgg gttagaaccg gcttgaacag cgggtgcaag agctgccatt gaagaattat 300 agggt 305 <210> SEQ ID NO 34 <211> LENGTH: 348 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 34 gtgacttgaa aacgcggtca ccatcatcat gagtctcctc aacaagccca agagtgagat 60 gaccccagag gagctgcaga agcgggagga ggaggagttt aacacggggc cactctccgt 120 gctcacgcag tcagtcaaaa acaacactca agtgctcatc aactgccgta acaacaagaa 180 gctcctgggc cgcgtgaagg cctttgacag gcactgcaac atggtgctgg agaacgtgaa 240 ggaaatgtgg acggaggtcc ccaagagcgg caagggcaag aagaagtcca agcccgtcaa 300 caaggaccgc tacatctcca agatgttcct gcgcggggac tctgtaat 348 <210> SEQ ID NO 35 <211> LENGTH: 366 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 35 ctggtggctg gggcaaaccc ccagtagatg agaccgggaa acccctctac ggggatgtgt 60 ttggaaccaa tgctgctgaa ttccagacca agactgagga agaagagatt gatcggaccc 120 cttgggggga gctagagcca tctgatgaag aatcttcaga agaagaggaa gaggaggaaa 180 gtgatgaaga taagccagat gagactggct tcattacccc tgcagacagt ggcctcatca 240 ctcctggagg gttctcgtca gtgccagctg gaatggagac ccccgaactc attgaattga 300 ggaaaaagaa gattgaggag gcgatggacg gaagtgagac gcctcagctg ttcactgtgt 360 tgccag 366 <210> SEQ ID NO 36 <211> LENGTH: 457 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 36 ctggcatctc tcggcgccct ggcgctactg ctgctgtccg gtctctcctg ctgctcagca 60 gaggcctgtg tggagcccca gatcacccct tcctactata ccacctcgga tgctgtcatt 120 tctactgaga ctgtcttcat cgtggagatc tccttgactt gcaagaacag ggtccagaac 180 atggctctct atgctgacgt cagtggaaaa caatttcctg tcacccgggg ccaggacgtg 240 ggacgttacc aggtgtcctg gagcctagat cacaagagcg cccatgcggg cacctatgag 300 gtccggttct ttgatgagga gtcctatagc ctcttgagga aggctcagag aaacaatgag 360 gacgtttctg tcatcccacc tctattcaca gtcagcgtag accatcgggg tacctggaac 420 gggccctggg tctccactga agtcctggcc gcagcca 457 <210> SEQ ID NO 37 <211> LENGTH: 548 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 37 gtgcatttat cagatcaaaa ccaacccggt cagcctcctc ccggccccgg ccggggggcg 60 ggcgccggcg gctttggtga ctctagataa cctcgggccg atcgcacgcc ccccgtggcg 120 gcgacgaccc attcgaacgt ccgccctatc aactttcgat ggtagtcgct gtgcctacca 180 tggtcacccg gggccaggac gtgggacgtt accaggtgtc ctggagccta gatcacaaga 240 gcgcccatgc gggcacctat gaggtccggt tctttgatga ggagtcctat agcctcttga 300 ggaaggctca gagaaacaat gaggacgttt ctgtcatccc acctctattc acagtcagcg 360 tagaccatcg gggtacctgg aacgggccct gggtctccac tgaagtcctg gccgcagcca 420 tcggactagt gatctactac cttgccttca gcgccaagag ccacatccag gcctgagggt 480 ggtgcccgcc cccacccttg cttctttgaa taaagagcta ttggctatcc tgaaaaaaaa 540 aaaaaaaa 548 <210> SEQ ID NO 38 <211> LENGTH: 432 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 38 tggagttgtg aagcaaccac attttcagga aaagcagata cccgaagagc caaagctgac 60 gttggatgag tcttgtgacc ttgatgttga aaatgaagaa gtcctgactt tgcaagaaac 120 tctggaagca cttagtctct ctgaatatgt tagcactttt gaaaaggaaa agattgatat 180 ggaatctctg cttatgtgta cagtggatga tctgaaggaa atggggatac cacttggacc 240 cagaaagaag atagctaact ttgtaaaaca taaagctgtc aaactggaag agaaaaaagc 300 agcatcggaa aagaaggcag cggtggccac ttcagcaaaa ggacaggagg aaagtgctca 360 gaaagctaaa gacatggctt ctcctccctc agactcgaac gagtccaaga ggagactccc 420 gcttggagcg tc 432 <210> SEQ ID NO 39 <211> LENGTH: 444 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 39 gagaactgga tatctgtgac caatcccacc caggctggtg cctgcggaaa cattctggag 60 agaaaccaga cccatgccat ctacataaac acgctctcct tagtcaacga tttcatcatc 120 agagacacca tcctcagcat caacttccag tgtgcctacc cactggacat gaaagtgagc 180 cttcaaatgg ccctgcagcc catcgtaagt tccctgaaca tcactgtgga tggggaggga 240 gagttcactg tcaggatggc cctctttcaa gaccaggact acacgtctcc ttatgaaggg 300 actgcagtca tgctgtctgt tgaatccatg ctctatgtgg gcaccatctt ggagagaggg 360 gacacgtccc gatttaacct gatgttgaaa atctgcacct tcctctgcct ctgctccagt 420 cttggatgca ccagcctcac cagc 444 <210> SEQ ID NO 40 <211> LENGTH: 873 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 40 ccaccgtacg ccggtgctgg gagtgcctgc cttctcttgt cttgaaaacc tcctctttgg 60 acccagcacc gccgtcctca cggtgatgtt ggactcagtg acacacagca ccttcctgcc 120 caacacgtcc ttctgcgacc ccctgatgtc gtggactgac ctgttcagca atgaagagta 180 ttaccctgcc tttgagcatc agacagcttg cgactcctac tggacatccg tccaccccga 240 atactggacg aagcgccacg tctgggaatg gctccagttc tgctgtgacc agtacaagct 300 ggacgccaac tgcatctctt tctgccattt caacatcagt ggcctgcagc tgtgcggcat 360 gacacaggag gagttcatgg agcggccggc gtctgtgggg agtatctgta ctttatcctc 420 cagagcatcc gctcacaagg ttactccttt tttaatgatc ctgatgagac caaggccaag 80 cctccagagt tctcatctat gggaatttgt gcgagatctg cttctatctc ctgaggaaaa 540 ctgcggcatt ctggaatggg aagctaggga acaaggtatt tttcgggtgg ttaaatcaga 600 agccctggcg aagatgtggg gacaaaggaa gaaaaatgac agaatgacgt acgaaaagct 660 gagcagagct ctgaggtact actataaaac cggaattttg gaacgggttg accgaagatt 720 agtgtacaaa tttggaaaaa atgcacatgg gtggcaggaa gacaagctat gatctgctcc 780 atcatccagc tcatgtaatg gatttctgtc ttttcaaaca atagattgca atagacattg 840 gaaagtcctt taaaaaaaaa aaaaaaaaaa aaa 873 <210> SEQ ID NO 41 <211> LENGTH: 380 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 41 ttgcaagtgg agaaaacata atatctggga tagaactagg taacattatg accaaagtgc 60 acggcaagag gtatgcctac aaatttgact tccacggcat cgcccaggct ctgcagccgc 120 atcccaccga gtcgtccatg tacaagtacc cttccgacat ctcctacgtg ccttcctacc 180 acacccacca acagaaggtg aactttgtcc ctccccaccc gtcctccatg cccgtcacgt 240 cctccagctt ctttggagcg gcgtcacaat actggacctc ccccacgggg ggcatctacc 300 ccaaccccaa cgtccctcgc catcccaaca cccacgtgcc ctcacactta ggcagctact 360 actagatgct tcctcatcgg 380 <210> SEQ ID NO 42 <211> LENGTH: 654 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 42 ccaccgtacg ccggtgctgg gagtgcctgc cttctcttgt cttgaaaacc tcctctttgg 60 acccagcacc gccgtcctca cggtgatgtt ggactcagtg acacacagca ccttcctgcc 120 caacacgtcc ttctgcgacc ccctgatgtc gtggactgac ctgttcagca atgaagagta 180 ttaccctgcc tttgagcatc agacagcttg cgactcctac tggacatccg tccaccccga 240 atactggacg aagcgccacg tctgggaatg gctccagttc tgctgtgacc agtacaagct 300 ggacgccaac tgcatctctt tctgccattt caacatcagt ggcctgcagc tgtgcggcat 360 gacacaggag gagttcatgg aggcggccgg cgtctgtggg gagtatctgt actttatcct 420 ccagagcatc cgctcacaag gttactcctt ttttaatgat cctgatgaga ccaaggccac 480 cctcaaagac tatgctgatt ccagttgctt gaaaacaagt ggcatcaaaa gtcaagactg 540 tcacagtcat agtcgaacaa gcctccagag ttctcatcta tgggaatttg tgcgagatct 600 gcttctatct cctgaggaaa actgcggcat tctggaatgg gaagataagg aaca 654 <210> SEQ ID NO 43 <211> LENGTH: 469 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 43 ggaggaggtg cctaatgtgg aatcttttct tggggaagga gctgttgacc ctaatgaccc 60 tgacaaggta aacacactaa atcaactctc caagactgag atttcccttt acctgaccag 120 caagtacgac ataggagatg gtgaagctat agatggccaa agcctcatga tcaagaccaa 180 aaaactgatc attgatgtga tccggaacca accaggaagc acactgacag aaatcttaga 240 gacaccagca agtgcaaaac aggagacaga tcatgcctca gacatggtga accgcgcggt 300 tttagattcc agaactcccg aagacatgaa gcagagccgg tctatggttg aagatgccca 360 gctgccccta gagcagaaaa agaggaaaat ccagaggaat cttcggacat tggaacagac 420 tggacacgtg tcatccaaaa acaaatacca agacattctc aataagatc 469 <210> SEQ ID NO 44 <211> LENGTH: 284 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 44 aaaacaccgt cagtgtggcc tcctggggac ccagtccaac ctttgtcgtc atcacagggg 60 aacagcgctg cagcacgtga ttcccagtgt gaaaacgcac caaagaaaga agtacctgta 120 agtccgggtc atcgaaaaac gccattcaca aaagacaaac attcaagccg cttggaggct 180 cacctcacaa gagatgagct acgggcaaaa gctctccata tcccattccc tgtagaaaag 240 atcattaacc tcccagttga ggacttcaat gaaatgatgt ccaa 284 <210> SEQ ID NO 45 <211> LENGTH: 315 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 45 ggaaaaacta cattaggcaa agaacttgca tcaagatcag gactgaaata cattaatgtg 60 ggtgatttag ctcgagaagt ttgatcaccg gatatcatgg agtctggcaa gatggcttct 120 cccaagagca tgccgaaaga tgcacagatg atggcacaaa tcctgaagga tatggggatt 180 acagaatatg aaccaagagt tataaatcag atgttggagt ttgccttccg atatgtgacc 240 acaattctag atgatgcaaa aatttattca agtcatgcta agaaagctac tgtcgatgca 300 gatgatgtgc gattg 315 <210> SEQ ID NO 46 <211> LENGTH: 433 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 46 ctcgggatga ttacaggcgg gatgatagag gtccccctca aagacccaaa ctgaacctaa 60 agcctcggag tactcctaag gaagatgatt cctccgctag cacctcccag tccagtcgtg 120 cagcctctat ctttggaggg gcaaagcctg ttgacacagc tgctagagaa cgagaagtag 180 aagagcggct acagaaggaa caggagaaac tgcagcgtca gctggatgag ccaaaactag 240 aacgacggcc tcgggagaga cacccaagct ggcgaagtga agaaactcag gaacgggaac 300 gatcgaggac aggaagtgag tcatcacaga ctgggacctc agccacatct ggcagaaatg 360 caagaagaag agagagtgag aagtctttag aaaatgaaac ccccaataaa gaggaagact 420 gtcagtctcc aac 433 <210> SEQ ID NO 47 <211> LENGTH: 412 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 47 tgactccggg ggcgcggcga ggagagagat gaggctgagc tgggtcttga cagtactgtc 60 catctgcctg agcgccctgg tcacggccac agggaccgag ggcaaacgga agctgcagat 120 cggagtcaag aaacgggtag accactgtcc catcaaatcg aggaaagggg acgtcctgca 180 catgcactat acggggaagc tagaagatgg aacagagttt gacagcagcc tgccccagaa 240 ccagcccttt gtcttctcct tgggcacagg ccaggtcatc aagggctggg accaggggct 300 gctagggatg tgtgaggggg aaaagcggaa gctggtgatt ccatcagagc tggggtatgg 360 agagcgggga gctcccccaa agattccagg tggtgcaacc ttggtgtttg ag 412 <210> SEQ ID NO 48 <211> LENGTH: 314 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 48 atggcggacg aggagaagct gccgcccggc tgggagaagc gtatgagccg cagttcaggc 60 cgggtgtact acttcaatca catcactaat gccagccagt gggagcggcc aagtggcaac 120 agcagtggca gcggcaaaaa cggacagggg gagcccacca gggtccgctg ctcacacctg 180 ctggtcaagc acagccagtc acggcggccc tcatcctggc ggcaggagaa gacgcctcct 240 tcgctctgcg gacaggggag atgagcgggc ccgtgttcac ggattcgggc atccacatca 300 tccttcgcac ggag 314 <210> SEQ ID NO 49 <211> LENGTH: 213 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 49 aaacaatatt attcagacct ggaggcagca ttttatccaa gaggaacaga tcctggagat 60 tgattgtacc atgcttaccc ctgagccagt tttaaagact tctggccatg tagacaaatt 120 tgctgacttc atggtgaaag atttaaaaaa tggagagtgt ttccgtgctg accatctatt 180 gaaagctcat ttacagaaat tgatgtctga taa 213 <210> SEQ ID NO 50 <211> LENGTH: 444 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 50 cccgtgaggc ggagaagcag gccagccccg cgctcgattg aacctgcatt ccccggcctc 60 ctgccaccat ggagtacctc atcggcatcc agggtcccga ctatgtcctt gtcgcctccg 120 accgggtggc tgctagcaat attgtccaga tgaaggatga tcatgacaag atgttcaaga 180 tgagtgaaaa aatcttactc ctgtgtgttg gagaggctgg agacactgta cagtttgcag 240 aatatattca gaaaaacgtg cagctctata agatgcgaaa tggttatgaa ctgtctccca 300 cggcagcagc taatttcact cgccgaaacc tggctgacta tcttcggagt cggaccccgt 360 atcatgtcaa cctcctcctg gccggctacg atgagcacga gggtccagca ctctactaca 420 tggactacct ggcagccttg gcaa 444 <210> SEQ ID NO 51 <211> LENGTH: 392 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 51 taggaaccgg ggggcctata caaccgtttc cagcctcggt ctgagtggac tatcctgcag 60 cgaccatgcc ccgtaaaggc acccagccct ccactgccca tcgcagagag gaagggccgc 120 cgcggtcccc ggacggcacc agcagcgacg cggaggccga ttccccgccc ggccgcgcga 180 ggagccaggc gctggccacc gcagaaactc caagtgagga aattgataat agaagtttag 240 aagagatttt gaatagcatc cctcctcccc acctcctgca atgaccaatg aacctggagc 300 tcctcgtctt atgataactc atattgtaaa ccagaacttc aaatcttacg ctggggaaaa 360 aattctggga cctttccata agcgattttc ct 392 <210> SEQ ID NO 52 <211> LENGTH: 426 <212> TYPE: DNA <213> ORGANISM: Bovine <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: (1)...(426) <223> OTHER INFORMATION: n = A,T,C or G <400> SEQUENCE: 52 gcgcagagat gcagatcttt gtgaagaccc tgacgggcaa gaccatcacc cttgaggtcg 60 agcccagtga caccattgag aatgtcaaag ccaaaatcca agacaaggag ggcatnccac 120 ctgaccagca gcggctgatc ttcgctggca aacagctgga ggatggccgc actctgtcag 180 attacaatat ccagaaagag tccaccctgc acttggtgct tcgtctgcga ggcggcatca 240 tcgagccttc cctccgccag ctcgctcaga aatacaactg gcgacaagat gatctgccgc 300 aagtgttacg cccgcctgca cccccgtgct gtcaactgcc gcaagaagaa gtgtggccac 360 accaacaacc tgcgccccaa gaagaaggtc aaataaagct cttccacctg cttctctttg 420 cccgca 426 <210> SEQ ID NO 53 <211> LENGTH: 328 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 53 tctcgcccgc cctcccgctc cctagcttgc tcgcgctttt gctcgcggtc tcctcgcgga 60 tcgaaggggt tctgaccaca gcttgtggct gagaagagcg acagaggcgg cgactcaaga 120 gaaacgaggc tgcagtggtg gtgggaagat gtcgggcgag gacgagcaac aggagcaaac 180 tatcgccgag gacctggtcg tgaccaagta taagatgggg ggcgacattg ctaaccgggt 240 acttcggtct ttggtggaag catcctgttc aggtgtgtcg gtactgagcc tgtgtgagaa 300 aggtgatgcc atgataatgg aagaaacg 328 <210> SEQ ID NO 54 <211> LENGTH: 240 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 54 taggaaaaca catgctactg aggcgggact gtggcccagt cgacaccaag actacagatg 60 acagaaatga gactttcagt tcattccttc cgctgctgaa caaggatccc ctcccccagg 120 acttttctgt gaagatggct tcgatcttca aggactttgt caccactata accggacata 180 tgattcgcag gaagaagcca gttggcgcat gtccgtcttt gccaataata tggtgcgagc 240 <210> SEQ ID NO 55 <211> LENGTH: 230 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 55 gaaatccaca gtgattggct actactccag gtcactagca gagtcttcac agaaggggac 60 cctctggcct tgaggtgtca tgcatggaag aatatgccgg tgtacaaaat gcttttctac 120 aaagatggca agccctttag gttttctagt caggattctg aattcaccat tctgcaaacc 180 aacttgagtc acaatggcat ctatcactgc tcgggcgaga gaaggcgtcg 230 <210> SEQ ID NO 56 <211> LENGTH: 192 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 56 accccaccca gcgtgaagca atgaccatgg ttgcagccca agtcatgggg aatcatgtcg 60 gtgttaccga cggaggcagc aatggacatt ttgagttgaa tgttttcacg ccaatgatga 120 ttaaaaatgt gttacactca gcccgactgc tgggggatgc atcggcttcc ttcacagaaa 180 actgcgtggt gg 192 <210> SEQ ID NO 57 <211> LENGTH: 433 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 57 ttgtcattca ccaaggctga aaactcaaag caaaataaac catgaggctg tctgtgactg 60 ccctgctggg tactctggcc ctttgctact acaaggccaa tgcaattgtc tgtccaacgt 120 ttgctgcgga tctgacagag ttcttctact ttcctgacct gctgtacagg ctgtcacttg 180 ccaagtacaa tgcacctcca gaagccgtgg ctgccaagat ggaagtgaag caatgcacgg 240 atagattctc agtcaaaaac agattaatca ttaccaacat actggggaaa atactgctga 300 attgtactgt cacagatgtg aaagctgtac taaatccttc ttctgcataa tcacctgatc 360 ttccattgaa aatgtagagg tttcaacatc ttgctcaata aatgatttac cctgcaaaaa 420 aaaaaaaaaa aaa 433 <210> SEQ ID NO 58 <211> LENGTH: 390 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 58 cgagcaccac taccgctgcg tggtgcagca cgcggggctg gcccagcccc tcacggtgga 60 gctggaatca ccagccagga cctcggtgcc agtggtgggg atcgtcatcg gcttattcct 120 gctcctgaca gtggctgcgg gaggagctct cctgtggaga aggatgagga aggggctgcc 180 agctccttgg atctctttcc gtggggagga tgtaggggcc ctcctgccca ctcccggcct 240 gtccaaggat ggtgaatctt aggataaaaa tgcattccca gcaactgccg atcatccccc 300 atcctggctg ttaccagcta atgtcctcag gtccttttca tgctgtgaga cctccgggaa 360 tcctggtatt tttgagcctc cggaaggagc 390 <210> SEQ ID NO 59 <211> LENGTH: 156 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 59 attcgcatca accataaaat ggatcctctg attggacagg cagcgcagcg gattggactg 60 agcagtcaga gctgttcagg cttctcccaa gtgaactcac gctctgggtt gacccgtacg 120 aagtgtccta cagaatcggc gaggatggct ccatct 156 <210> SEQ ID NO 60 <211> LENGTH: 134 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 60 caacaaacga ccaacactgt ggaagagccc ttggatctca tccggctcag cctggacgag 60 cgcatctacg tgaagatgag gaacgacaga gagctccgag gcaggttgca tgcttatgat 120 cagcatttaa atat 134 <210> SEQ ID NO 61 <211> LENGTH: 125 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 61 ttcaaacgct atcatgaccc caactttgtc cctgcggcct ttgtctgttc taagtgtggg 60 aaaacattta cacgccggaa tactatggca agacatgcgg ataattgtgc tggtccagat 120 ggtgt 125 <210> SEQ ID NO 62 <211> LENGTH: 458 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 62 aagaattcgg cacgagtgta aatgcggccg gtggaccaac cccaagccag agaggtctgt 60 ctgacctggc tttgtgtgga ccagcggcga accagtgtgc agtgccggcc aaggacaggg 120 tggactgcgg ctaccccgag gtcacccccg agcagtgcaa caaccgcggc tgctgcttcg 180 actccagcat ccacggggtg ccctggtgct tcaagcccct gcaggaagca gaatgcacct 240 tctgaagcca cgtggccgcc cgacacccag ggaggggatc tccgtacttg ggtaccctgc 300 ccgcccaccc agtgctcatc cctctgcttc tctcaaactg ctcctggcca ggcctgaacc 360 aaatgcctgg ggcctgatgt cttaaagaat aaagctcccg tgctcagcat gaggacaggt 420 cttcattcct aaaaaacaaa aaaaaaaaaa aaaaaaaa 458 <210> SEQ ID NO 63 <211> LENGTH: 397 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 63 ctgccttcac atccctcacc ccagagccgg ccactgaaga cacatgagct tcgagatcca 60 gtgttgtctg cagccattgc cacgaagatg gccaagttcc acggcatgga gatgcctttc 120 actaaggagc cccactggct attcgggacc atggagcggt acttaaagca gatccaggac 180 ctgcccccta ccagccttcc ccagaggtaa agaaagatga gaccatctcc caagaggagc 240 agaggaaact ggaagcagat ttgctggtgg aagctaatcg gtatgccctg gcatctcatt 300 tcttttgggg tctctggtcc atccttcagg catccatgtc cactatagaa tttggttact 360 tggagtatgc gcagtctcgg ttccagttct acttcca 397 <210> SEQ ID NO 64 <211> LENGTH: 423 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 64 tacacgaggg accacgcggg tagcttcctg acggagtccc ggagcctcag cacccacctg 60 ctcctcctct acggcctcca gggcctgctg accttcgggt acctggtgct gctgtcgcgc 120 atcggcgagc gcatggccgt ggatctacgg agggcgcttt tctgcaacct gctccgccaa 180 gacatcgagt tcttcgatgc taagaggcat cgccttgttc caggggctct ccaacatcgc 240 cttcaactgc atggtcttgg gcaccctgtt tgttgggggc tcactcgtgg ccgggcagca 300 gctgacgggg ggagacctca tgtccttcct ggtggcctct cagactgtgc agaggtgaga 360 gtgggccgtt ctcttcccga ggggcccagc tggggcaggg ggcgccagtc ttctgtggat 420 acg 423 <210> SEQ ID NO 65 <211> LENGTH: 539 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 65 ggcacgagct cgaaccctca cacagacacc tggaaaagcc acggcctggt ggaggtggcc 60 agttactgcg aagaaagtag ggggaacaac cagtgggttc cctacatctc cctccaggag 120 cgctgagacc ccgccgggca tcggaaactt gctgcggaaa acacaaaacc acataaatat 180 ttgacccccc ctccctccca gaacaacccc ccctcaacaa cccaacccgt gagaccatcg 240 ggggcaggat cgctggagac tgaagacagg acccgggcca gcaggagagg ggacctggga 300 gctcaggcct ggtgacagag cagatgcagg agttggggag gtgcttgctt cccccaccaa 360 ggagggcctg ggctccacac ttcgggggtg gggtgggact gactgcagcc cccacccttc 420 ttgagaccgg agctgacatc tgcaaaaaac gggccttggt tggccgaggg tcggcaccca 480 ggccaggaca gtactttggg acttgggagc aagggctcat gttgcttctg tacccatga 539 <210> SEQ ID NO 66 <211> LENGTH: 180 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 66 gacttggaga cttctttgga gacccaggaa acccttcttc tgaatttact ccctcaggaa 60 gtaaagatgg aaaatacgag ttgttgacag cagcaaatga agttatcgct gaagagatca 120 aagatctaat gaccaaaagt gacatagagg gtcaacacac agagactctg ctggcaggat 180 <210> SEQ ID NO 67 <211> LENGTH: 464 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 67 atcacctgct ctggaaccag cagcaatgtt ggagatggcg attatgtgag ttggttccaa 60 cagatcccag gatcgggccc cagaacagtc atctttggtg cgactcagcg accctctggg 120 gtctccgagc gattctccgg ctccaggtct ggcaacacag ccaccctaac catcagctcg 180 ctccaggccg aggacgaggc ggattatttc tgttcatctc ccgacaccac taacaatgtt 240 gctttcggca gcgggaccac cctgagcgtc ctgagacagc gactggaaat cgaaaggcag 300 ttacagctgc gaggtcacgc acgacgggag caccgtgacg aagacagtga agccctcaga 360 gtgtccttag ggcctggacc cccaccctcg ggggccctct ggcccacacc ccctccccca 420 cctctccatg gacccctgag cccctaccca ggtcgcctac acca 464 <210> SEQ ID NO 68 <211> LENGTH: 669 <212> TYPE: DNA <213> ORGANISM: Bovine <400> SEQUENCE: 68 ccgaggcgca gcagaggagg gtccaggaga cggaggtgaa gccatgtggc agctgctgct 60 ccccctggcc ctggggctgg gcaccatggg cttgggcagg gcggagctca cgacggccca 120 gcaccggggc ctgcaggtgg ccctggagga gttccacaag catccacccg tgctgtgggc 180 cttccaggtg accagcgtgg acaatgcggc agacacgctc ttcccggctg ggcagtttgt 240 gaggctggag ttcaagctcc agcagacgag ctgtcggaag aaagactgga ggaaagaaga 300 ctgcaaagtc aagcccaacg ggagaaagcg gaaatgcctg gcctgcatca agctggactc 360 aaaagatcaa gtcctgggcc ggatggtgca ctgtcccata cagactcagg agctggacga 420 cgcccaggac gcccagtgca gcagggtgga gcgcgccggc gaggaccccc acagctacta 80 cctccccgga cagtttgcct tcatcaaagc cttgtccccc tgagctgagg cctggcagaa 540 gtcacccggc ttcctggaag gaagggaggt cgccagtgaa agcccgcctc cctcctctgg 600 gcccggggag gggccacccc ctgacccctg agctaataaa gctgtgctca gctgaaaaaa 660 aaaaaaaaa 669 <210> SEQ ID NO 69 <211> LENGTH: 89 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 69 Lys Met Lys Val Leu Thr Phe Ala Cys Lys Val Gln Lys Lys Asp Pro 1 5 10 15 Lys Asp Trp Ala Ala Gln Tyr Arg Lys Ala Met Glu Ala Asp Met Lys 20 25 30 Ala Ala Ala Glu Ala Ala Leu Asp Ser Lys Ala Arg Ala Asp Ile Arg 35 40 45 Ala Gln Met Gly Ile Gly Leu Gly Ser Glu Asn Ala Ala Gly Pro Cys 50 55 60 Asn Trp Asp Glu Ala Asp Ile Gly Pro Trp Ala Lys Ala Arg Ile Gln 65 70 75 80 Ala Gly Ala Glu Ala Lys Ala Lys Ala 85 <210> SEQ ID NO 70 <211> LENGTH: 143 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 70 Ile Cys Arg Ser Ile Tyr Ala Val Phe Gly Ala Glu Ile Asn Leu Lys 1 5 10 15 Gly Ile Pro Val Tyr Arg Phe Ile Leu Pro Ser Phe Ala Phe Ala Ser 20 25 30 Pro Phe Gln Asn Pro Asp Asn His Cys Phe Cys Thr Glu Lys Ile Ile 35 40 45 Ser Lys Asn Cys Thr Leu Tyr Gly Val Leu Asp Ile Gly Lys Cys Lys 50 55 60 Glu Gly Lys Pro Val Tyr Ile Ser Leu Pro His Phe Leu His Gly Ser 65 70 75 80 Pro Glu Leu Ala Glu Pro Ile Glu Ser Leu Ser Pro Asn Glu Glu Glu 85 90 95 His Ser Thr Tyr Leu Asp Val Glu Pro Ile Thr Gly Phe Thr Leu Arg 100 105 110 Phe Ala Lys Arg Leu Gln Val Asn Met Leu Val Lys Pro Ala Lys Lys 115 120 125 Ile Glu Ala Leu Lys Asn Leu Lys His Asn Tyr Ile Val Pro Ile 130 135 140 <210> SEQ ID NO 71 <211> LENGTH: 82 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 71 Arg Asp Leu Gly Lys Arg Ile Gln Asp Pro Arg Gly Met Tyr Arg Cys 1 5 10 15 Gly Glu Asn Thr Gln Gln Leu Ile Leu Gln Val Tyr Tyr Arg Met Cys 20 25 30 Gln Asn Cys Val Glu Leu Asp Thr Ala Thr Leu Ala Gly Met Ile Ile 35 40 45 Thr Asp Ile Ile Ala Thr Val Leu Leu Ala Leu Gly Val Tyr Cys Phe 50 55 60 Ala Gly His Glu Thr Gly Arg Phe Ser Arg Ala Ala Asp Thr Gln Ala 65 70 75 80 Leu Met <210> SEQ ID NO 72 <211> LENGTH: 113 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 72 Cys Arg Cys Gln Pro Gly Tyr Tyr Gly Asp Gly Phe Gln Cys Thr Pro 1 5 10 15 Glu Pro Thr Gln Arg Pro Arg Thr Val Cys Glu Arg Trp Arg Glu Ser 20 25 30 Leu Leu Glu His Tyr Gly Gly Thr Pro Arg Asp Asp Gln Tyr Val Pro 35 40 45 Gln Cys Asp Asp Leu Gly His Phe Thr Pro Leu Gln Cys His Gly Lys 50 55 60 Ser Asp Phe Cys Trp Cys Val Asp Gln Asp Gly Arg Glu Val Gln Gly 65 70 75 80 Thr Arg Ser Gln Pro Gly Ile Thr Pro Ala Cys Ile Pro Thr Val Ala 85 90 95 Pro Pro Thr Val Arg Pro Thr Pro Arg Pro Asp Val Thr Pro Pro Pro 100 105 110 Val SEQ ID NO 73 <211> LENGTH: 70 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 73 Met Cys Asp Lys Glu Phe Met Trp Ala Leu Lys Asn Gly Asp Leu Asp 1 5 10 15 Glu Val Lys Asp Tyr Val Ala Lys Gly Glu Asp Val Asn Arg Thr Leu 20 25 30 Glu Gly Gly Arg Lys Pro Leu His Tyr Ala Ala Asp Cys Gly Gln Leu 35 40 45 Glu Ile Leu Glu Phe Leu Leu Leu Lys Gly Ala Asp Ile Asn Ala Pro 50 55 60 Asp Lys His His Ile Thr 65 70 <210> SEQ ID NO 74 <211> LENGTH: 236 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 74 Met Asn Ile Phe Asp Arg Lys Ile Asn Phe Asp Ala Leu Phe Lys Phe 1 5 10 15 Ser His Ile Thr Pro Ser Thr Gln Gln His Leu Lys Lys Val Tyr Ala 20 25 30 Ser Phe Ala Leu Cys Met Phe Val Ala Ala Ala Gly Ala Tyr Ile His 35 40 45 Val Val Thr His Phe Ile Gln Ala Gly Leu Leu Ser Ala Leu Gly Ser 50 55 60 Leu Gly Leu Met Ile Trp Leu Met Ala Thr Pro His Ser His Glu Thr 65 70 75 80 Glu Gln Lys Arg Leu Gly Leu Leu Ala Gly Phe Ala Phe Leu Thr Gly 85 90 95 Val Gly Leu Gly Pro Ala Leu Asp Leu Cys Ile Ala Ile Asn Pro Ser 100 105 110 Ile Leu Pro Thr Ala Phe Met Gly Thr Ala Met Ile Phe Thr Cys Phe 115 120 125 Thr Leu Ser Ala Leu Tyr Ala Arg Arg Arg Ser Tyr Leu Phe Leu Gly 130 135 140 Gly Ile Leu Met Ser Ala Met Ser Leu Met Leu Leu Ser Ser Leu Gly 145 150 155 160 Asn Leu Phe Phe Gly Ser Val Trp Leu Phe Gln Ala Asn Leu Tyr Met 165 170 175 Gly Leu Val Val Met Cys Gly Phe Val Leu Phe Asp Thr Gln Leu Ile 180 185 190 Ile Glu Lys Ala Glu Asn Gly Asp Lys Asp Tyr Ile Trp His Cys Val 195 200 205 Asp Leu Phe Leu Asp Phe Val Thr Leu Phe Arg Lys Leu Met Met Ile 210 215 220 Leu Ala Met Asn Glu Lys Asp Lys Lys Lys Lys Lys 225 230 235 <210> SEQ ID NO 75 <211> LENGTH: 161 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 75 Cys Thr Cys Leu Asp Gly Ser Val Gly Cys Val Pro Leu Cys Ser Val 1 5 10 15 Asp Val Arg Leu Pro Ser Pro Asp Cys Pro Phe Pro Arg Arg Val Lys 20 25 30 Leu Pro Gly Lys Cys Cys Glu Glu Trp Val Cys Asp Glu Pro Lys Glu 35 40 45 His Thr Val Val Gly Pro Ala Leu Ala Ala Tyr Arg Pro Glu Asp Thr 50 55 60 Phe Gly Pro Asp Pro Thr Met Ile Arg Ala Asn Cys Leu Val Gln Thr 65 70 75 80 Thr Glu Trp Ser Ala Cys Ser Lys Thr Cys Gly Met Gly Ile Ser Thr 85 90 95 Arg Val Thr Asn Asp Asn Ala Phe Cys Arg Leu Glu Lys Gln Ser Arg 100 105 110 Leu Cys Met Val Arg Pro Cys Glu Ala Asp Leu Glu Glu Asn Ile Lys 115 120 125 Lys Gly Lys Lys Cys Ile Arg Thr Pro Lys Ile Ser Lys Pro Ile Lys 130 135 140 Phe Glu Leu Ser Gly Cys Thr Ser Met Lys Thr Tyr Arg Ala Lys Phe 145 150 155 160 Cys <210> SEQ ID NO 76 <211> LENGTH: 120 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 76 Ala Leu Lys Lys Val Lys Phe Gln Ala Lys Leu Glu His Glu Tyr Ile 1 5 10 15 Gln Asn Phe Lys Ile Leu Gln Ala Gly Phe Lys Arg Met Gly Val Asp 20 25 30 Lys Ile Ile Pro Val Asp Lys Leu Val Lys Gly Lys Phe Gln Asp Asn 35 40 45 Phe Glu Phe Val Gln Trp Phe Lys Lys Phe Phe Asp Ala Asn Tyr Asp 50 55 60 Gly Lys Glu Tyr Asp Pro Val Ala Ala Arg Gln Gly Gln Glu Thr Ala 65 70 75 80 Met Ala Pro Ser Leu Val Ala Pro Ala Leu Asn Lys Pro Lys Lys Pro 85 90 95 Leu Ser Ser Ser Ser Ala Ala Pro Gln Arg Pro Ile Thr Thr His Arg 100 105 110 Thr Thr Ala Thr Pro Lys Ala Gly 115 120 <210> SEQ ID NO 77 <211> LENGTH: 144 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 77 Lys Thr His Lys Asn Pro Ala Leu Lys Ala Gln Ser Gly Leu Ile Arg 1 5 10 15 Ser Gly Pro Lys Pro Phe Ser Ala Ser Lys Pro Asp Pro Pro Lys Pro 20 25 30 Val Ala Lys Lys Glu Pro Ala Leu Leu Glu Leu Glu Gly Lys Lys Trp 35 40 45 Arg Val Glu Asn Gln Glu Asn Val Ser Asn Leu Met Ile Glu Asp Thr 50 55 60 Glu Leu Lys Gln Val Ala Tyr Ile Phe Lys Cys Val Asn Ser Thr Leu 65 70 75 80 Gln Ile Lys Gly Lys Ile Asn Ser Ile Thr Val Asp Asn Cys Lys Lys 85 90 95 Leu Gly Leu Val Phe Asp Asp Val Val Gly Ile Val Glu Ile Ile Asn 100 105 110 Ser Lys Asp Val Lys Val Gln Val Met Gly Lys Val Pro Thr Ile Ser 115 120 125 Ile Asn Lys Thr Asp Gly Cys His Val Tyr Leu Ser Lys Asn Ser Leu 130 135 140 <210> SEQ ID NO 78 <211> LENGTH: 100 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 78 Glu Arg Arg Arg Val Ala Gln Gln Lys Gln Gln Gln Leu Glu Gln Glu 1 5 10 15 Gln Phe His Ala Phe Glu Glu Met Ile Arg Asn Gln Glu Leu Glu Lys 20 25 30 Glu Arg Leu Lys Ile Val Gln Glu Phe Gly Lys Val Asp Pro Val Leu 35 40 45 Gly Gly Pro Leu Val Pro Asp Leu Glu Thr Pro Ser Leu Asp Val Phe 50 55 60 Pro Thr Val Pro Ala Ile Pro Thr Gln Pro Ser Asp Cys Asn Ala Ala 65 70 75 80 Val Arg Leu Ala Lys Pro Pro Val Val Asp Arg Ser Leu Lys Pro Gly 85 90 95 Ala Leu Asn Asn 100 <210> SEQ ID NO 79 <211> LENGTH: 136 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 79 Tyr Phe Lys Gly Ile Met Gln Asp Val Gln Leu Leu Val Met Pro Gln 1 5 10 15 Gly Phe Ile Ala Gln Cys Pro Asp Leu Asn Arg Thr Cys Pro Thr Cys 20 25 30 Asn Asp Phe His Gly Leu Val Gln Lys Ile Met Glu Leu Gln Asp Ile 35 40 45 Leu Ala Lys Thr Ser Ala Lys Leu Ser Arg Ala Glu Gln Arg Met Asn 50 55 60 Arg Leu Asp Gln Cys Tyr Cys Glu Arg Thr Cys Thr Met Lys Gly Thr 65 70 75 80 Thr Tyr Arg Glu Phe Glu Ser Trp Thr Asp Gly Cys Lys Asn Cys Thr 85 90 95 Cys Leu Asn Gly Thr Ile Gln Cys Glu Thr Leu Ile Cys Pro Asn Pro 100 105 110 Asp Cys Pro Leu Lys Ser Ala Pro Ala Tyr Val Asp Gly Lys Cys Cys 115 120 125 Lys Glu Cys Lys Ser Ile Cys Gln 130 135 <210> SEQ ID NO 80 <211> LENGTH: 127 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 80 Arg Val Pro Gly Arg His Gly Tyr Ala Ala Glu Phe Ser Pro Tyr Leu 1 5 10 15 Pro Gly Arg Leu Ala Cys Ala Ala Ser Gln His Tyr Gly Ile Ala Gly 20 25 30 Ser Gly Thr Leu Leu Ile Leu Asp Gln Asn Glu Ser Gly Leu Arg Leu 35 40 45 Phe Arg Ser Phe Asp Trp Asn Asp Gly Leu Phe Asp Val Thr Trp Ser 50 55 60 Glu Asn Asn Glu His Val Leu Val Thr Cys Ser Gly Asp Gly Ser Leu 65 70 75 80 Gln Leu Trp Asp Thr Ala Arg Ala Thr Gly Pro Leu Gln Val Phe Lys 85 90 95 Glu His Thr Gln Glu Val Tyr Ser Val Asp Trp Ser Gln Thr Arg Gly 100 105 110 Glu Gln Leu Val Val Ser Gly Ser Trp Asp Gln Thr Val Lys Leu 115 120 125 <210> SEQ ID NO 81 <211> LENGTH: 151 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 81 Leu Arg Pro Gln Met Ala Ser Ser Lys Asn Tyr Gly Ser Pro Leu Ile 1 5 10 15 Ser Gly Ser Thr Pro Lys His Glu Arg Gly Ser Pro Ser His Ser Lys 20 25 30 Ser Pro Ala Tyr Thr Pro Gln Asn Leu Asp Ser Glu Ser Glu Ser Gly 35 40 45 Ser Ser Ile Ala Glu Lys Ser Tyr Gln Asn Ser Pro Ser Ser Asp Asp 50 55 60 Gly Ile Arg Pro Leu Pro Glu Tyr Ser Thr Glu Lys His Lys Lys His 65 70 75 80 Lys Lys Glu Lys Lys Lys Val Lys Asp Lys Asp Arg Asp Arg Asp Lys 85 90 95 Asp Arg Asp Lys Lys Lys Ser His Ser Ile Lys Pro Glu Ser Trp Ser 100 105 110 Lys Ser Pro Ile Ser Ser Asp Gln Ser Leu Ser Met Thr Ser Asn Thr 115 120 125 Ile Leu Ser Thr Asp Arg Pro Ser Arg Leu Ser Pro Asp Phe Met Ile 130 135 140 Gly Glu Glu Asp Asp Asp Leu 145 150 <210> SEQ ID NO 82 <211> LENGTH: 159 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 82 Trp Lys Lys Asn Thr Pro Phe Leu Tyr Asp Leu Val Met Thr His Ala 1 5 10 15 Leu Gln Trp Pro Ser Leu Thr Val Gln Trp Leu Pro Glu Val Thr Lys 20 25 30 Pro Glu Gly Lys Asp Tyr Ala Leu His Trp Leu Gly Leu Gly Thr His 35 40 45 Thr Ser Asp Glu Gln Asn His Leu Val Val Ala Arg Val His Ile Pro 50 55 60 Asn Asp Asp Ala Gln Phe Asp Ala Ser His Cys Asp Ser Glu Lys Gly 65 70 75 80 Glu Phe Gly Gly Phe Gly Ser Val Thr Gly Lys Ile Glu Cys Glu Ile 85 90 95 Lys Ile Asn His Glu Gly Glu Val Asn Arg Ala Arg Tyr Met Pro Gln 100 105 110 Asn Pro His Ile Ile Ala Thr Lys Thr Pro Ser Ser Asp Val Leu Val 115 120 125 Phe Asp Tyr Thr Lys His Pro Ala Lys Pro Asp Pro Ser Gly Glu Cys 130 135 140 Asn Pro Asp Leu Arg Leu Arg Gly His Gln Lys Glu Gly Tyr Gly 145 150 155 <210> SEQ ID NO 83 <211> LENGTH: 106 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 83 Ser His Glu His Pro Ser Thr Gln Asp Gln Gly Asn His Leu Ala Glu 1 5 10 15 Glu Cys Leu Ser Ser Asp Glu Gly Thr Pro Pro Ser Ile Lys Lys Ile 20 25 30 Ile His Val Leu Glu Lys Val Gln Tyr Leu Glu Gln Glu Val Glu Glu 35 40 45 Phe Val Gly Lys Lys Thr Asp Lys Ala Tyr Trp Leu Leu Glu Glu Met 50 55 60 Leu Thr Lys Glu Leu Leu Glu Leu Asp Ser Val Glu Thr Gly Gly Gln 65 70 75 80 Asp Ser Val Arg Gln Ala Arg Lys Glu Ala Val Cys Lys Ile Gln Ala 85 90 95 Ile Leu Glu Lys Leu Glu Lys Lys Gly Leu 100 105 <210> SEQ ID NO 84 <211> LENGTH: 125 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 84 Met Gln Ala Leu Val Leu Leu Leu Trp Thr Gly Ala Leu Leu Gly Phe 1 5 10 15 Gly Arg Cys Gln Asn Ala Gly Gln Glu Ala Gly Ser Leu Thr Pro Glu 20 25 30 Ser Thr Gly Ala Pro Val Glu Glu Glu Asp Pro Phe Phe Lys Val Pro 35 40 45 Val Asn Lys Leu Ala Ala Ala Val Ser Asn Phe Gly Tyr Asp Leu Tyr 50 55 60 Arg Val Arg Ser Gly Glu Ser Pro Thr Ala Asn Val Leu Leu Ser Pro 65 70 75 80 Leu Ser Val Ala Thr Ala Leu Ser Ala Leu Ser Leu Gly Ala Glu Gln 85 90 95 Arg Thr Glu Ser Asn Ile His Arg Ala Leu Tyr Tyr Asp Leu Ile Ser 100 105 110 Asn Pro Asp Ile His Gly Thr Tyr Lys Asp Leu Leu Ala 115 120 125 <210> SEQ ID NO 85 <211> LENGTH: 128 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 85 Met Pro Glu Glu Val His His Gly Glu Glu Glu Val Glu Thr Phe Ala 1 5 10 15 Phe Gln Ala Glu Ile Ala Gln Leu Met Ser Leu Ile Ile Asn Thr Phe 20 25 30 Tyr Ser Asn Lys Glu Ile Phe Leu Arg Glu Leu Ile Ser Asn Ala Ser 35 40 45 Asp Ala Leu Asp Lys Ile Arg Tyr Glu Ser Leu Thr Asp Pro Ser Lys 50 55 60 Leu Asp Ser Gly Lys Glu Leu Lys Ile Asp Ile Ile Pro Asn Pro Gln 65 70 75 80 Glu Arg Thr Leu Thr Leu Val Asp Thr Gly Ile Gly Met Thr Lys Ala 85 90 95 Asp Leu Val Asn Asn Leu Gly Thr Ile Ala Lys Ser Gly Thr Lys Ala 100 105 110 Phe Met Glu Ala Leu Gln Ala Gly Ala Asp Ile Ser Met Ile Gly Gln 115 120 125 <210> SEQ ID NO 86 <211> LENGTH: 118 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 86 Arg Lys Lys Arg Lys Ile Arg Glu Glu Ile Glu His Phe Gly Ile Lys 1 5 10 15 Val Tyr Gln Phe Pro Asp Cys Asp Ser Asp Glu Asp Glu Asp Phe Lys 20 25 30 Ser Gln Asp Leu Ala Leu Lys Glu Ser Ile Pro Phe Ala Val Ile Gly 35 40 45 Ser Asn Thr Val Val Glu Ala Arg Gly Arg Arg Val Arg Gly Arg Leu 50 55 60 Tyr Pro Trp Gly Ile Val Glu Val Glu Asn Pro Gly His Cys Asp Phe 65 70 75 80 Val Lys Leu Arg Thr Met Leu Val Arg Thr His Met Gln Asp Leu Lys 85 90 95 Asp Val Thr Arg Glu Thr His Tyr Glu Asn Tyr Arg Ala Gln Cys Ile 100 105 110 Gln Ser Met Thr Arg Leu 115 <210> SEQ ID NO 87 <211> LENGTH: 112 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 87 Glu Asp Leu Arg Asn Lys Ile His Thr Ala Thr Val Asp Asn Ala Asn 1 5 10 15 Leu Leu Leu Gln Ile Asp Asn Ala Arg Leu Ala Ala Asp Asp Phe Arg 20 25 30 Thr Lys Phe Glu Thr Glu Gln Ala Leu Arg Val Ser Val Glu Ala Asp 35 40 45 Ile Asn Gly Leu Arg Arg Val Leu Asp Glu Leu Thr Leu Ala Arg Ala 50 55 60 Asp Leu Glu Met Gln Ile Glu Asn Leu Lys Glu Glu Leu Ala Tyr Leu 65 70 75 80 Arg Lys Asn His Glu Glu Glu Met Lys Ala Leu Arg Gly Gln Val Gly 85 90 95 Gly Glu Ile Asn Val Glu Met Asp Ala Ala Pro Gly Val Asp Leu Ser 100 105 110 <210> SEQ ID NO 88 <211> LENGTH: 217 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 88 Lys Tyr Glu Asp Glu Ile Asn His Arg Thr Ala Ala Glu Asn Glu Phe 1 5 10 15 Val Val Leu Lys Lys Asp Val Asp Val Ala Tyr Met Asn Lys Val Glu 20 25 30 Leu Glu Ala Lys Val Asp Thr Leu Asn Asp Glu Ile Asn Phe Leu Arg 35 40 45 Thr Leu Tyr Glu Gln Glu Leu Lys Glu Leu Gln Ser Glu Val Ser Asp 50 55 60 Thr Ser Val Val Leu Ser Met Asp Asn Asn Arg Ser Leu Asp Leu Asp 65 70 75 80 Ser Ile Ile Ala Glu Val Lys Ala Gln Tyr Glu Glu Ile Ala Asn Arg 85 90 95 Ser Arg Ala Glu Ala Glu Ala Cys Tyr Gln Thr Lys Phe Glu Thr Leu 100 105 110 Gln Ala Gln Ala Gly Lys His Gly Asp Asp Leu Arg Asn Thr Arg Asn 115 120 125 Glu Ile Ala Asp Met Asn Arg Ala Val Gln Arg Leu Gln Ala Glu Ile 130 135 140 Asp Ser Val Lys Asn Gln Arg Ser Lys Leu Glu Ala Ala Ile Ala Asp 145 150 155 160 Ala Glu Gln Arg Gly Glu Leu Ala Val Lys Asp Ala Arg Ala Lys Gln 165 170 175 Glu Asp Leu Glu Ala Ala Leu Gln Lys Ala Lys Gln Asp Met Thr Arg 180 185 190 Gln Leu Arg Glu Tyr Gln Glu Leu Met Asn Val Lys Leu Ala Leu Asp 195 200 205 Ile Glu Ile Ala Thr Tyr Arg Lys Leu 210 215 <210> SEQ ID NO 89 <211> LENGTH: 134 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 89 Met Val Pro Val Leu Leu Ala Leu Leu Leu Leu Leu Gly Pro Ala Val 1 5 10 15 Ser Glu Glu Thr Gln Ala Gly Asn Tyr Ser Leu Ser Phe Leu Tyr Thr 20 25 30 Gly Leu Ser Lys Pro Arg Glu Gly Phe Pro Ser Phe Gln Ala Val Ala 35 40 45 Tyr Leu Asn Asp Gln Pro Phe Phe His Tyr Asn Ser Glu Gly Arg Arg 50 55 60 Ala Glu Pro Leu Ala Pro Trp Ser Gln Val Glu Gly Met Glu Asp Trp 65 70 75 80 Glu Lys Glu Ser Ala Leu Gln Arg Ala Arg Glu Asp Ile Phe Met Glu 85 90 95 Thr Leu Ser Asp Ile Met Asp Tyr Tyr Lys Asp Arg Glu Gly Ser His 100 105 110 Thr Phe Gln Gly Ala Phe Gly Cys Glu Leu Arg Asn Asn Glu Ser Ser 115 120 125 Gly Ala Phe Trp Gly Tyr 130 <210> SEQ ID NO 90 <211> LENGTH: 116 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 90 Phe Gly Ser Gly Thr Thr Leu Thr Val Leu Gly Gln Pro Lys Ser Ala 1 5 10 15 Pro Ser Val Thr Leu Phe Pro Pro Ser Lys Glu Glu Leu Asp Thr Asn 20 25 30 Lys Ala Thr Leu Val Cys Leu Ile Ser Asp Phe Tyr Pro Gly Ser Val 35 40 45 Thr Val Val Trp Lys Ala Asp Gly Ser Thr Ile Thr Arg Asp Val Lys 50 55 60 Thr Thr Arg Pro Ser Lys Gln Ser Asn Ser Lys Tyr Ala Ala Ser Ser 65 70 75 80 Tyr Leu Ser Leu Thr Asp Ser Asp Trp Lys Ser Lys Gly Ser Tyr Ser 85 90 95 Cys Glu Val Thr His Asp Gly Ser Thr Val Thr Lys Thr Val Lys Pro 100 105 110 Ser Glu Cys Pro 115 <210> SEQ ID NO 91 <211> LENGTH: 124 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 91 Asp Val Glu Val His Thr Ala Arg Thr Lys Pro Arg Glu Glu Gln Phe 1 5 10 15 Asn Ser Thr Tyr Arg Val Val Ser Ala Leu Arg Ile Gln His Gln Asp 20 25 30 Trp Leu Gln Gly Lys Glu Phe Lys Cys Lys Val Asn Asn Lys Gly Leu 35 40 45 Pro Ala Pro Ile Val Arg Thr Ile Ser Arg Thr Lys Gly Gln Ala Arg 50 55 60 Glu Pro Gln Val Tyr Val Leu Ala Pro Pro Arg Glu Glu Leu Ser Lys 65 70 75 80 Ser Thr Leu Ser Leu Thr Cys Leu Ile Thr Gly Phe Tyr Pro Glu Glu 85 90 95 Ile Asp Val Glu Trp Gln Arg Asn Gly Gln Pro Glu Ser Glu Asp Lys 100 105 110 Tyr His Thr Thr Ala Pro Gln Leu Asp Ala Asp Gly 115 120 <210> SEQ ID NO 92 <211> LENGTH: 205 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 92 Pro Lys Pro Lys Asp Thr Leu Thr Ile Ser Gly Thr Pro Glu Val Thr 1 5 10 15 Cys Val Val Val Asp Val Gly His Asp Asp Pro Glu Val Lys Phe Ser 20 25 30 Trp Phe Val Asp Asn Val Glu Val Asn Thr Ala Thr Thr Lys Pro Arg 35 40 45 Glu Glu Gln Phe Asn Ser Thr Tyr Arg Val Val Ser Ala Leu Arg Ile 50 55 60 Gln His Gln Asp Trp Thr Gly Gly Lys Glu Phe Thr Cys Lys Val His 65 70 75 80 Asn Glu Gly Leu Pro Ala Pro Ile Val Arg Thr Ile Ser Arg Thr Lys 85 90 95 Gly Gln Ala Arg Glu Pro Gln Val Tyr Val Leu Ala Pro Pro Gln Glu 100 105 110 Glu Leu Ser Lys Ser Thr Val Ser Leu Thr Cys Met Val Thr Ser Phe 115 120 125 Tyr Pro Asp Tyr Ile Ala Val Glu Trp Gln Arg Asn Gly Gln Pro Glu 130 135 140 Ser Glu Asp Lys Tyr Gly Thr Thr Pro Pro Gln Leu Asp Ala Asp Ser 145 150 155 160 Ser Tyr Phe Leu Tyr Ser Lys Leu Arg Val Asp Arg Asn Ser Trp Gln 165 170 175 Glu Gly Asp Thr Tyr Thr Cys Val Val Met His Glu Ala Leu His Asn 180 185 190 His Tyr Thr Gln Lys Ser Thr Ser Lys Ser Ala Gly Lys 195 200 205 <210> SEQ ID NO 93 <211> LENGTH: 84 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 93 Met Pro Tyr Leu Leu Ile Ser Thr Gln Ile Arg Met Glu Val Gly Pro 1 5 10 15 Thr Val Val Gly Asp Glu His Ser Asp Pro Glu Leu Met Gln His Leu 20 25 30 Gly Ala Ser Lys Arg Ser Val Leu Gly Asn Asn Phe Ser Glu Tyr Tyr 35 40 45 Val Asn Asp Pro Pro Arg Ile Val Leu Asp Lys Leu Glu Arg Arg Gly 50 55 60 Phe Arg Val Leu Ser Met Thr Gly Val Gly Gln Thr Leu Val Trp Cys 65 70 75 80 Leu His Lys Glu <210> SEQ ID NO 94 <211> LENGTH: 220 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 94 Glu Arg Gln Glu Val Val Pro His Arg Arg Gly Gln Asp Cys Arg Leu 1 5 10 15 Glu His Pro His Gly Pro Asp Arg Asn Gln Thr Gly Ser Cys Ala Phe 20 25 30 Asp Glu Phe Phe Ser Gln Ser Cys Ala Pro Gly Ala Asp Pro Lys Ser 35 40 45 Arg Leu Cys Ala Leu Cys Ala Gly Asp Asp Gln Gly Leu Asp Lys Cys 50 55 60 Val Pro Asn Ser Lys Glu Lys Tyr Tyr Gly Tyr Thr Gly Ala Phe Arg 65 70 75 80 Cys Leu Ala Glu Asp Val Gly Asp Val Ala Phe Val Lys Asn Asp Thr 85 90 95 Val Trp Glu Asn Thr Asn Gly Glu Ser Thr Ala Asp Trp Ala Lys Asn 100 105 110 Leu Asn Arg Glu Asp Phe Arg Leu Leu Cys Leu Asp Gly Thr Arg Lys 115 120 125 Pro Val Thr Glu Ala Gln Ser Cys His Leu Ala Val Ala Pro Asn His 130 135 140 Ala Val Val Ser Arg Ser Asp Arg Ala Ala His Val Lys Gln Val Leu 145 150 155 160 Leu His Gln Gln Ala Leu Phe Gly Lys Asn Gly Lys Asn Cys Pro Asp 165 170 175 Lys Phe Cys Leu Phe Lys Ser Glu Thr Lys Asn Leu Leu Phe Asn Asp 180 185 190 Asn Thr Glu Cys Leu Ala Lys Leu Gly Gly Arg Pro Thr Tyr Glu Asp 195 200 205 Ile Trp Gly Gln Ser Met Ser Arg Pro Leu Pro Thr 210 215 220 <210> SEQ ID NO 95 <211> LENGTH: 248 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 95 Pro Gly Pro Gly Pro Gly Pro Gly Ser Asn Leu Thr Ser Ala Pro Gly 1 5 10 15 Pro Ser Thr Thr Thr Arg Ser Leu Thr Ala Cys Pro Glu Glu Ser Pro 20 25 30 Leu Leu Val Gly Pro Met Leu Ile Glu Phe Asn Ile Pro Val Asp Leu 35 40 45 Lys Leu Val Glu His Gln Asn Pro Lys Val Lys Leu Gly Gly Arg Tyr 50 55 60 Thr Pro Thr Asp Cys Ile Ser Pro His Lys Val Ala Ile Ile Ile Pro 65 70 75 80 Phe Arg Asn Arg Gln Glu His Leu Lys Tyr Trp Leu Tyr Tyr Leu His 85 90 95 Pro Ile Leu Gln Arg Gln Gln Leu Asp Tyr Gly Ile Tyr Val Ile Asn 100 105 110 Gln Ala Gly Glu Ser Met Phe Asn Arg Ala Lys Leu Leu Asn Val Gly 115 120 125 Phe Lys Glu Ala Leu Lys Asp Tyr Asp Tyr Asn Cys Phe Val Phe Ser 130 135 140 Asp Val Asp Leu Ile Pro Met Asn Asp His Asn Thr Tyr Arg Cys Phe 145 150 155 160 Ser Gln Pro Arg His Ile Ser Val Ala Met Asp Lys Phe Gly Phe Ser 165 170 175 Leu Pro Tyr Val Gln Tyr Phe Gly Gly Val Ser Ala Leu Ser Lys Gln 180 185 190 Gln Phe Leu Ser Ile Asn Gly Phe Pro Asn Asn Tyr Trp Gly Trp Gly 195 200 205 Gly Glu Asp Asp Asp Ile Tyr Lys Gln Ile Ser Phe Arg Gly Met Ser 210 215 220 Val Ser Arg Pro Asn Ala Val Ile Gly Lys Cys Arg Met Ile Arg Thr 225 230 235 240 Arg Glu Thr Lys Lys Asn Glu Pro 245 <210> SEQ ID NO 96 <211> LENGTH: 158 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 96 Ser Ile Gly Ile Gln Lys Pro Val Gly His Val Asp Ile Tyr Pro Asn 1 5 10 15 Gly Gly Thr Phe Gln Pro Gly Cys Asn Ile Gly Glu Ala Leu Arg Val 20 25 30 Ile Ala Glu Arg Gly Leu Gly Asp Val Asp Gln Leu Val Lys Cys Ser 35 40 45 His Glu Arg Ser Val His Leu Phe Ile Asp Ser Leu Leu Asn Glu Glu 50 55 60 Asn Pro Ser Lys Ala Tyr Arg Cys Asn Ser Lys Glu Ala Phe Glu Lys 65 70 75 80 Gly Leu Cys Leu Ser Cys Arg Lys Asn Arg Cys Asn Asn Met Gly Tyr 85 90 95 Glu Ile Asn Lys Val Arg Ala Lys Arg Ser Ser Lys Met Tyr Leu Lys 100 105 110 Thr Arg Ser Gln Met Pro Tyr Lys Val Phe His Tyr Gln Val Lys Ile 115 120 125 His Phe Ser Gly Thr Glu Ser Asn Thr Tyr Thr Asn Gln Ala Phe Glu 130 135 140 Ile Ser Leu Tyr Gly Thr Val Ala Glu Ser Glu Asn Ile Pro 145 150 155 <210> SEQ ID NO 97 <211> LENGTH: 150 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 97 Ala Ala Val Ala Met Ala Pro Ile Lys Val Gly Asp Ala Ile Pro Ser 1 5 10 15 Val Glu Val Phe Glu Lys Glu Pro Gly Asn Lys Val Asn Leu Ala Glu 20 25 30 Leu Phe Lys Gly Lys Lys Gly Val Leu Phe Gly Leu Pro Gly Ala Phe 35 40 45 Thr Pro Gly Gly Ser Lys Thr His Leu Pro Gly Phe Val Glu Gln Ala 50 55 60 Asp Ala Leu Lys Ala Lys Gly Ile Gln Val Val Ala Cys Leu Thr Val 65 70 75 80 Asn Asp Val Phe Val Thr Glu Glu Trp Ala Arg Ala His Lys Ala Glu 85 90 95 Gly Lys Val Arg Leu Leu Ala Asp Pro Ser Gly Thr Phe Gly Lys Glu 100 105 110 Thr Asp Leu Leu Leu Asp Asp Ser Leu Leu Phe Leu Phe Gly Asn His 115 120 125 Arg Leu Lys Arg Phe Ser Met Val Ile Glu Asp Gly Ile Val Lys Ser 130 135 140 Leu Asn Val Glu Pro Asp 145 150 <210> SEQ ID NO 98 <211> LENGTH: 119 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 98 Met Ala Asn Gly Tyr Thr Tyr Glu Asp Tyr Gln Asp Thr Ala Lys Trp 1 5 10 15 Leu Leu Ser His Thr Glu Gln Arg Pro Gln Val Ala Val Ile Cys Gly 20 25 30 Ser Gly Leu Gly Gly Leu Val Asn Lys Leu Thr Gln Ala Gln Thr Phe 35 40 45 Asp Tyr Ser Glu Ile Pro Asn Phe Pro Glu Ser Thr Val Pro Gly His 50 55 60 Ala Gly Arg Leu Val Phe Gly Ile Leu Asn Gly Arg Ala Cys Val Met 65 70 75 80 Met Gln Gly Arg Phe His Met Tyr Glu Gly Tyr Pro Phe Trp Lys Val 85 90 95 Thr Phe Pro Val Arg Val Phe Arg Leu Leu Gly Val Glu Thr Leu Val 100 105 110 Val Thr Thr Gln Leu Arg Ala 115 <210> SEQ ID NO 99 <211> LENGTH: 94 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 99 Ile Gly Glu Gly Glu Asp Leu Ile Lys Trp Lys Ala Leu Phe Glu Glu 1 5 10 15 Val Pro Glu Leu Leu Thr Glu Thr Glu Lys Lys Glu Trp Ile Asp Lys 20 25 30 Leu Asn Glu Val Ser Ile Ser Ser Asp Ala Phe Phe Pro Phe Arg Asp 35 40 45 Asn Val Asp Arg Ala Lys Val Ser Gly Val Ala Tyr Ile Ala Ala Pro 50 55 60 Ser Gly Ser Ala Ala Asp Lys Val Val Ile Glu Ala Cys Asp Glu Leu 65 70 75 80 Gly Ile Ile Leu Ala His Thr Asn Leu Arg Leu Phe His His 85 90 <210> SEQ ID NO 100 <211> LENGTH: 137 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 100 Met Pro Pro Tyr Thr Ile Val Tyr Phe Pro Val Gln Gly Arg Cys Glu 1 5 10 15 Ala Met Arg Met Leu Leu Ala Asp Gln Gly Gln Ser Trp Lys Glu Glu 20 25 30 Val Val Ala Met Gln Ser Trp Leu Gln Gly Pro Leu Lys Ala Ser Cys 35 40 45 Leu Tyr Gly Gln Leu Pro Lys Phe Gln Asp Gly Asp Leu Thr Leu Tyr 50 55 60 Gln Ser Asn Ala Ile Leu Arg His Leu Gly Arg Thr Leu Gly Leu Tyr 65 70 75 80 Gly Lys Asp Gln Gln Glu Ala Ala Leu Val Asp Met Val Asn Asp Gly 85 90 95 Val Glu Asp Leu Arg Cys Lys Tyr Val Ser Leu Ile Tyr Thr Asn Tyr 100 105 110 Glu Ala Gly Lys Glu Asp Tyr Val Lys Ala Leu Pro Gln His Leu Lys 115 120 125 Pro Phe Glu Thr Leu Leu Ser Gln Asn 130 135 <210> SEQ ID NO 101 <211> LENGTH: 96 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 101 Ile Gln Arg Ala His Gln Asn Thr Trp Glu Val Tyr Pro Pro Phe Leu 1 5 10 15 Phe Phe Leu Ala Val Gly Gly Val Tyr His Pro Arg Ile Val Ser Gly 20 25 30 Leu Gly Leu Ala Trp Ile Val Gly Arg Val Leu Tyr Ala Tyr Gly Tyr 35 40 45 Tyr Thr Gly Glu Pro Arg Lys Arg Gln Arg Gly Ala Leu Ser Phe Ile 50 55 60 Ala Leu Ile Gly Leu Met Gly Thr Thr Val Cys Ser Ala Phe Gln His 65 70 75 80 Leu Gly Trp Val Arg Thr Gly Leu Asn Ser Gly Cys Lys Ser Cys His 85 90 95 <210> SEQ ID NO 102 <211> LENGTH: 106 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 102 Met Ser Leu Leu Asn Lys Pro Lys Ser Glu Met Thr Pro Glu Glu Leu 1 5 10 15 Gln Lys Arg Glu Glu Glu Glu Phe Asn Thr Gly Pro Leu Ser Val Leu 20 25 30 Thr Gln Ser Val Lys Asn Asn Thr Gln Val Leu Ile Asn Cys Arg Asn 35 40 45 Asn Lys Lys Leu Leu Gly Arg Val Lys Ala Phe Asp Arg His Cys Asn 50 55 60 Met Val Leu Glu Asn Val Lys Glu Met Trp Thr Glu Val Pro Lys Ser 65 70 75 80 Gly Lys Gly Lys Lys Lys Ser Lys Pro Val Asn Lys Asp Arg Tyr Ile 85 90 95 Ser Lys Met Phe Leu Arg Gly Asp Ser Val 100 105 <210> SEQ ID NO 103 <211> LENGTH: 121 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 103 Gly Gly Trp Gly Lys Pro Pro Val Asp Glu Thr Gly Lys Pro Leu Tyr 1 5 10 15 Gly Asp Val Phe Gly Thr Asn Ala Ala Glu Phe Gln Thr Lys Thr Glu 20 25 30 Glu Glu Glu Ile Asp Arg Thr Pro Trp Gly Glu Leu Glu Pro Ser Asp 35 40 45 Glu Glu Ser Ser Glu Glu Glu Glu Glu Glu Glu Ser Asp Glu Asp Lys 50 55 60 Pro Asp Glu Thr Gly Phe Ile Thr Pro Ala Asp Ser Gly Leu Ile Thr 65 70 75 80 Pro Gly Gly Phe Ser Ser Val Pro Ala Gly Met Glu Thr Pro Glu Leu 85 90 95 Ile Glu Leu Arg Lys Lys Lys Ile Glu Glu Ala Met Asp Gly Ser Glu 100 105 110 Thr Pro Gln Leu Phe Thr Val Leu Pro 115 120 <210> SEQ ID NO 104 <211> LENGTH: 152 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 104 Leu Ala Ser Leu Gly Ala Leu Ala Leu Leu Leu Leu Ser Gly Leu Ser 1 5 10 15 Cys Cys Ser Ala Glu Ala Cys Val Glu Pro Gln Ile Thr Pro Ser Tyr 20 25 30 Tyr Thr Thr Ser Asp Ala Val Ile Ser Thr Glu Thr Val Phe Ile Val 35 40 45 Glu Ile Ser Leu Thr Cys Lys Asn Arg Val Gln Asn Met Ala Leu Tyr 50 55 60 Ala Asp Val Ser Gly Lys Gln Phe Pro Val Thr Arg Gly Gln Asp Val 65 70 75 80 Gly Arg Tyr Gln Val Ser Trp Ser Leu Asp His Lys Ser Ala His Ala 85 90 95 Gly Thr Tyr Glu Val Arg Phe Phe Asp Glu Glu Ser Tyr Ser Leu Leu 100 105 110 Arg Lys Ala Gln Arg Asn Asn Glu Asp Val Ser Val Ile Pro Pro Leu 115 120 125 Phe Thr Val Ser Val Asp His Arg Gly Thr Trp Asn Gly Pro Trp Val 130 135 140 Ser Thr Glu Val Leu Ala Ala Ala 145 150 <210> SEQ ID NO 105 <211> LENGTH: 105 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 105 Met Val Val Ala Val Pro Thr Met Val Thr Arg Gly Gln Asp Val Gly 1 5 10 15 Arg Tyr Gln Val Ser Trp Ser Leu Asp His Lys Ser Ala His Ala Gly 20 25 30 Thr Tyr Glu Val Arg Phe Phe Asp Glu Glu Ser Tyr Ser Leu Leu Arg 35 40 45 Lys Ala Gln Arg Asn Asn Glu Asp Val Ser Val Ile Pro Pro Leu Phe 50 55 60 Thr Val Ser Val Asp His Arg Gly Thr Trp Asn Gly Pro Trp Val Ser 65 70 75 80 Thr Glu Val Leu Ala Ala Ala Ile Gly Leu Val Ile Tyr Tyr Leu Ala 85 90 95 Phe Ser Ala Lys Ser His Ile Gln Ala 100 105 <210> SEQ ID NO 106 <211> LENGTH: 143 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 106 Gly Val Val Lys Gln Pro His Phe Gln Glu Lys Gln Ile Pro Glu Glu 1 5 10 15 Pro Lys Leu Thr Leu Asp Glu Ser Cys Asp Leu Asp Val Glu Asn Glu 20 25 30 Glu Val Leu Thr Leu Gln Glu Thr Leu Glu Ala Leu Ser Leu Ser Glu 35 40 45 Tyr Val Ser Thr Phe Glu Lys Glu Lys Ile Asp Met Glu Ser Leu Leu 50 55 60 Met Cys Thr Val Asp Asp Leu Lys Glu Met Gly Ile Pro Leu Gly Pro 65 70 75 80 Arg Lys Lys Ile Ala Asn Phe Val Lys His Lys Ala Val Lys Leu Glu 85 90 95 Glu Lys Lys Ala Ala Ser Glu Lys Lys Ala Ala Val Ala Thr Ser Ala 100 105 110 Lys Gly Gln Glu Glu Ser Ala Gln Lys Ala Lys Asp Met Ala Ser Pro 115 120 125 Pro Ser Asp Ser Asn Glu Ser Lys Arg Arg Leu Pro Leu Gly Ala 130 135 140 <210> SEQ ID NO 107 <211> LENGTH: 148 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 107 Glu Asn Trp Ile Ser Val Thr Asn Pro Thr Gln Ala Gly Ala Cys Gly 1 5 10 15 Asn Ile Leu Glu Arg Asn Gln Thr His Ala Ile Tyr Ile Asn Thr Leu 20 25 30 Ser Leu Val Asn Asp Phe Ile Ile Arg Asp Thr Ile Leu Ser Ile Asn 35 40 45 Phe Gln Cys Ala Tyr Pro Leu Asp Met Lys Val Ser Leu Gln Met Ala 50 55 60 Leu Gln Pro Ile Val Ser Ser Leu Asn Ile Thr Val Asp Gly Glu Gly 65 70 75 80 Glu Phe Thr Val Arg Met Ala Leu Phe Gln Asp Gln Asp Tyr Thr Ser 85 90 95 Pro Tyr Glu Gly Thr Ala Val Met Leu Ser Val Glu Ser Met Leu Tyr 100 105 110 Val Gly Thr Ile Leu Glu Arg Gly Asp Thr Ser Arg Phe Asn Leu Met 115 120 125 Leu Lys Ile Cys Thr Phe Leu Cys Leu Cys Ser Ser Leu Gly Cys Thr 130 135 140 Ser Leu Thr Ser 145 <210> SEQ ID NO 108 <211> LENGTH: 228 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 108 Met Leu Asp Ser Val Thr His Ser Thr Phe Leu Pro Asn Thr Ser Phe 1 5 10 15 Cys Asp Pro Leu Met Ser Trp Thr Asp Leu Phe Ser Asn Glu Glu Tyr 20 25 30 Tyr Pro Ala Phe Glu His Gln Thr Ala Cys Asp Ser Tyr Trp Thr Ser 35 40 45 Val His Pro Glu Tyr Trp Thr Lys Arg His Val Trp Glu Trp Leu Gln 50 55 60 Phe Cys Cys Asp Gln Tyr Lys Leu Asp Ala Asn Cys Ile Ser Phe Cys 65 70 75 80 His Phe Asn Ile Ser Gly Leu Gln Leu Cys Gly Met Thr Gln Glu Glu 85 90 95 Phe Met Glu Arg Pro Ala Ser Val Gly Ser Ile Cys Thr Leu Ser Ser 100 105 110 Arg Ala Ser Ala His Lys Val Thr Pro Phe Leu Met Ile Leu Met Arg 115 120 125 Pro Arg Pro Ser Leu Gln Ser Ser His Leu Trp Glu Phe Val Arg Asp 130 135 140 Leu Leu Leu Ser Pro Glu Glu Asn Cys Gly Ile Leu Glu Trp Glu Ala 145 150 155 160 Arg Glu Gln Gly Ile Phe Arg Val Val Lys Ser Glu Ala Leu Ala Lys 165 170 175 Met Trp Gly Gln Arg Lys Lys Asn Asp Arg Met Thr Tyr Glu Lys Leu 180 185 190 Ser Arg Ala Leu Arg Tyr Tyr Tyr Lys Thr Gly Ile Leu Glu Arg Val 195 200 205 Asp Arg Arg Leu Val Tyr Lys Phe Gly Lys Asn Ala His Gly Trp Gln 210 215 220 Glu Asp Lys Leu 225 <210> SEQ ID NO 109 <211> LENGTH: 120 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 109 Ala Ser Gly Glu Asn Ile Ile Ser Gly Ile Glu Leu Gly Asn Ile Met 1 5 10 15 Thr Lys Val His Gly Lys Arg Tyr Ala Tyr Lys Phe Asp Phe His Gly 20 25 30 Ile Ala Gln Ala Leu Gln Pro His Pro Thr Glu Ser Ser Met Tyr Lys 35 40 45 Tyr Pro Ser Asp Ile Ser Tyr Val Pro Ser Tyr His Thr His Gln Gln 50 55 60 Lys Val Asn Phe Val Pro Pro His Pro Ser Ser Met Pro Val Thr Ser 65 70 75 80 Ser Ser Phe Phe Gly Ala Ala Ser Gln Tyr Trp Thr Ser Pro Thr Gly 85 90 95 Gly Ile Tyr Pro Asn Pro Asn Val Pro Arg His Pro Asn Thr His Val 100 105 110 Pro Ser His Leu Gly Ser Tyr Tyr 115 120 <210> SEQ ID NO 110 <211> LENGTH: 217 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 110 His Arg Thr Pro Val Leu Gly Val Pro Ala Phe Ser Cys Leu Glu Asn 1 5 10 15 Leu Leu Phe Gly Pro Ser Thr Ala Val Leu Thr Val Met Leu Asp Ser 20 25 30 Val Thr His Ser Thr Phe Leu Pro Asn Thr Ser Phe Cys Asp Pro Leu 35 40 45 Met Ser Trp Thr Asp Leu Phe Ser Asn Glu Glu Tyr Tyr Pro Ala Phe 50 55 60 Glu His Gln Thr Ala Cys Asp Ser Tyr Trp Thr Ser Val His Pro Glu 65 70 75 80 Tyr Trp Thr Lys Arg His Val Trp Glu Trp Leu Gln Phe Cys Cys Asp 85 90 95 Gln Tyr Lys Leu Asp Ala Asn Cys Ile Ser Phe Cys His Phe Asn Ile 100 105 110 Ser Gly Leu Gln Leu Cys Gly Met Thr Gln Glu Glu Phe Met Glu Ala 115 120 125 Ala Gly Val Cys Gly Glu Tyr Leu Tyr Phe Ile Leu Gln Ser Ile Arg 130 135 140 Ser Gln Gly Tyr Ser Phe Phe Asn Asp Pro Asp Glu Thr Lys Ala Thr 145 150 155 160 Leu Lys Asp Tyr Ala Asp Ser Ser Cys Leu Lys Thr Ser Gly Ile Lys 165 170 175 Ser Gln Asp Cys His Ser His Ser Arg Thr Ser Leu Gln Ser Ser His 180 185 190 Leu Trp Glu Phe Val Arg Asp Leu Leu Leu Ser Pro Glu Glu Asn Cys 195 200 205 Gly Ile Leu Glu Trp Glu Asp Lys Glu 210 215 <210> SEQ ID NO 111 <211> LENGTH: 156 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 111 Glu Glu Val Pro Asn Val Glu Ser Phe Leu Gly Glu Gly Ala Val Asp 1 5 10 15 Pro Asn Asp Pro Asp Lys Val Asn Thr Leu Asn Gln Leu Ser Lys Thr 20 25 30 Glu Ile Ser Leu Tyr Leu Thr Ser Lys Tyr Asp Ile Gly Asp Gly Glu 35 40 45 Ala Ile Asp Gly Gln Ser Leu Met Ile Lys Thr Lys Lys Leu Ile Ile 50 55 60 Asp Val Ile Arg Asn Gln Pro Gly Ser Thr Leu Thr Glu Ile Leu Glu 65 70 75 80 Thr Pro Ala Ser Ala Lys Gln Glu Thr Asp His Ala Ser Asp Met Val 85 90 95 Asn Arg Ala Val Leu Asp Ser Arg Thr Pro Glu Asp Met Lys Gln Ser 100 105 110 Arg Ser Met Val Glu Asp Ala Gln Leu Pro Leu Glu Gln Lys Lys Arg 115 120 125 Lys Ile Gln Arg Asn Leu Arg Thr Leu Glu Gln Thr Gly His Val Ser 130 135 140 Ser Lys Asn Lys Tyr Gln Asp Ile Leu Asn Lys Ile 145 150 155 <210> SEQ ID NO 112 <211> LENGTH: 94 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 112 Lys Thr Pro Ser Val Trp Pro Pro Gly Asp Pro Val Gln Pro Leu Ser 1 5 10 15 Ser Ser Gln Gly Asn Ser Ala Ala Ala Arg Asp Ser Gln Cys Glu Asn 20 25 30 Ala Pro Lys Lys Glu Val Pro Val Ser Pro Gly His Arg Lys Thr Pro 35 40 45 Phe Thr Lys Asp Lys His Ser Ser Arg Leu Glu Ala His Leu Thr Arg 50 55 60 Asp Glu Leu Arg Ala Lys Ala Leu His Ile Pro Phe Pro Val Glu Lys 65 70 75 80 Ile Ile Asn Leu Pro Val Glu Asp Phe Asn Glu Met Met Ser 85 90 <210> SEQ ID NO 113 <211> LENGTH: 73 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 113 Met Glu Ser Gly Lys Met Ala Ser Pro Lys Ser Met Pro Lys Asp Ala 1 5 10 15 Gln Met Met Ala Gln Ile Leu Lys Asp Met Gly Ile Thr Glu Tyr Glu 20 25 30 Pro Arg Val Ile Asn Gln Met Leu Glu Phe Ala Phe Arg Tyr Val Thr 35 40 45 Thr Ile Leu Asp Asp Ala Lys Ile Tyr Ser Ser His Ala Lys Lys Ala 50 55 60 Thr Val Asp Ala Asp Asp Val Arg Leu 65 70 <210> SEQ ID NO 114 <211> LENGTH: 143 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 114 Arg Asp Asp Tyr Arg Arg Asp Asp Arg Gly Pro Pro Gln Arg Pro Lys 1 5 10 15 Leu Asn Leu Lys Pro Arg Ser Thr Pro Lys Glu Asp Asp Ser Ser Ala 20 25 30 Ser Thr Ser Gln Ser Ser Arg Ala Ala Ser Ile Phe Gly Gly Ala Lys 35 40 45 Pro Val Asp Thr Ala Ala Arg Glu Arg Glu Val Glu Glu Arg Leu Gln 50 55 60 Lys Glu Gln Glu Lys Leu Gln Arg Gln Leu Asp Glu Pro Lys Leu Glu 65 70 75 80 Arg Arg Pro Arg Glu Arg His Pro Ser Trp Arg Ser Glu Glu Thr Gln 85 90 95 Glu Arg Glu Arg Ser Arg Thr Gly Ser Glu Ser Ser Gln Thr Gly Thr 100 105 110 Ser Ala Thr Ser Gly Arg Asn Ala Arg Arg Arg Glu Ser Glu Lys Ser 115 120 125 Leu Glu Asn Glu Thr Pro Asn Lys Glu Glu Asp Cys Gln Ser Pro 130 135 140 <210> SEQ ID NO 115 <211> LENGTH: 137 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 115 Asp Ser Gly Gly Ala Ala Arg Arg Glu Met Arg Leu Ser Trp Val Leu 1 5 10 15 Thr Val Leu Ser Ile Cys Leu Ser Ala Leu Val Thr Ala Thr Gly Thr 20 25 30 Glu Gly Lys Arg Lys Leu Gln Ile Gly Val Lys Lys Arg Val Asp His 35 40 45 Cys Pro Ile Lys Ser Arg Lys Gly Asp Val Leu His Met His Tyr Thr 50 55 60 Gly Lys Leu Glu Asp Gly Thr Glu Phe Asp Ser Ser Leu Pro Gln Asn 65 70 75 80 Gln Pro Phe Val Phe Ser Leu Gly Thr Gly Gln Val Ile Lys Gly Trp 85 90 95 Asp Gln Gly Leu Leu Gly Met Cys Glu Gly Glu Lys Arg Lys Leu Val 100 105 110 Ile Pro Ser Glu Leu Gly Tyr Gly Glu Arg Gly Ala Pro Pro Lys Ile 115 120 125 Pro Gly Gly Ala Thr Leu Val Phe Glu 130 135 <210> SEQ ID NO 116 <211> LENGTH: 87 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 116 Met Ala Asp Glu Glu Lys Leu Pro Pro Gly Trp Glu Lys Arg Met Ser 1 5 10 15 Arg Ser Ser Gly Arg Val Tyr Tyr Phe Asn His Ile Thr Asn Ala Ser 20 25 30 Gln Trp Glu Arg Pro Ser Gly Asn Ser Ser Gly Ser Gly Lys Asn Gly 35 40 45 Gln Gly Glu Pro Thr Arg Val Arg Cys Ser His Leu Leu Val Lys His 50 55 60 Ser Gln Ser Arg Arg Pro Ser Ser Trp Arg Gln Glu Lys Thr Pro Pro 65 70 75 80 Ser Leu Cys Gly Gln Gly Arg 85 <210> SEQ ID NO 117 <211> LENGTH: 70 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 117 Asn Asn Ile Ile Gln Thr Trp Arg Gln His Phe Ile Gln Glu Glu Gln 1 5 10 15 Ile Leu Glu Ile Asp Cys Thr Met Leu Thr Pro Glu Pro Val Leu Lys 20 25 30 Thr Ser Gly His Val Asp Lys Phe Ala Asp Phe Met Val Lys Asp Leu 35 40 45 Lys Asn Gly Glu Cys Phe Arg Ala Asp His Leu Leu Lys Ala His Leu 50 55 60 Gln Lys Leu Met Ser Asp 65 70 <210> SEQ ID NO 118 <211> LENGTH: 125 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 118 Met Glu Tyr Leu Ile Gly Ile Gln Gly Pro Asp Tyr Val Leu Val Ala 1 5 10 15 Ser Asp Arg Val Ala Ala Ser Asn Ile Val Gln Met Lys Asp Asp His 20 25 30 Asp Lys Met Phe Lys Met Ser Glu Lys Ile Leu Leu Leu Cys Val Gly 35 40 45 Glu Ala Gly Asp Thr Val Gln Phe Ala Glu Tyr Ile Gln Lys Asn Val 50 55 60 Gln Leu Tyr Lys Met Arg Asn Gly Tyr Glu Leu Ser Pro Thr Ala Ala 65 70 75 80 Ala Asn Phe Thr Arg Arg Asn Leu Ala Asp Tyr Leu Arg Ser Arg Thr 85 90 95 Pro Tyr His Val Asn Leu Leu Leu Ala Gly Tyr Asp Glu His Glu Gly 100 105 110 Pro Ala Leu Tyr Tyr Met Asp Tyr Leu Ala Ala Leu Ala 115 120 125 <210> SEQ ID NO 119 <211> LENGTH: 68 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 119 Met Pro Arg Lys Gly Thr Gln Pro Ser Thr Ala His Arg Arg Glu Glu 1 5 10 15 Gly Pro Pro Arg Ser Pro Asp Gly Thr Ser Ser Asp Ala Glu Ala Asp 20 25 30 Ser Pro Pro Gly Arg Ala Arg Ser Gln Ala Leu Ala Thr Ala Glu Thr 35 40 45 Pro Ser Glu Glu Ile Asp Asn Arg Ser Leu Glu Glu Ile Leu Asn Ser 50 55 60 Ile Pro Pro Pro 65 <210> SEQ ID NO 120 <211> LENGTH: 139 <212> TYPE: PRT <213> ORGANISM: Bovine <220> FEATURE: <221> NAME/KEY: VARIANT <222> LOCATION: (1)...(139) <223> OTHER INFORMATION: Xaa = Any Amino Acid <400> SEQUENCE: 120 Met Gln Ile Phe Val Lys Thr Leu Thr Gly Lys Thr Ile Thr Leu Glu 1 5 10 15 Val Glu Pro Ser Asp Thr Ile Glu Asn Val Lys Ala Lys Ile Gln Asp 20 25 30 Lys Glu Gly Xaa Pro Pro Asp Gln Gln Arg Leu Ile Phe Ala Gly Lys 35 40 45 Gln Leu Glu Asp Gly Arg Thr Leu Ser Asp Tyr Asn Ile Gln Lys Glu 50 55 60 Ser Thr Leu His Leu Val Leu Arg Leu Arg Gly Gly Ile Ile Glu Pro 65 70 75 80 Ser Leu Arg Gln Leu Ala Gln Lys Tyr Asn Trp Arg Gln Asp Asp Leu 85 90 95 Pro Gln Val Leu Arg Pro Pro Ala Pro Pro Cys Cys Gln Leu Pro Gln 100 105 110 Glu Glu Val Trp Pro His Gln Gln Pro Ala Pro Gln Glu Glu Gly Gln 115 120 125 Ile Lys Leu Phe His Leu Leu Leu Phe Ala Arg 130 135 <210> SEQ ID NO 121 <211> LENGTH: 60 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 121 Met Ser Gly Glu Asp Glu Gln Gln Glu Gln Thr Ile Ala Glu Asp Leu 1 5 10 15 Val Val Thr Lys Tyr Lys Met Gly Gly Asp Ile Ala Asn Arg Val Leu 20 25 30 Arg Ser Leu Val Glu Ala Ser Cys Ser Gly Val Ser Val Leu Ser Leu 35 40 45 Cys Glu Lys Gly Asp Ala Met Ile Met Glu Glu Thr 50 55 60 <210> SEQ ID NO 122 <211> LENGTH: 79 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 122 Gly Lys His Met Leu Leu Arg Arg Asp Cys Gly Pro Val Asp Thr Lys 1 5 10 15 Thr Thr Asp Asp Arg Asn Glu Thr Phe Ser Ser Phe Leu Pro Leu Leu 20 25 30 Asn Lys Asp Pro Leu Pro Gln Asp Phe Ser Val Lys Met Ala Ser Ile 35 40 45 Phe Lys Asp Phe Val Thr Thr Ile Thr Gly His Met Ile Arg Arg Lys 50 55 60 Lys Pro Val Gly Ala Cys Pro Ser Leu Pro Ile Ile Trp Cys Glu 65 70 75 <210> SEQ ID NO 123 <211> LENGTH: 76 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 123 Glu Ile His Ser Asp Trp Leu Leu Leu Gln Val Thr Ser Arg Val Phe 1 5 10 15 Thr Glu Gly Asp Pro Leu Ala Leu Arg Cys His Ala Trp Lys Asn Met 20 25 30 Pro Val Tyr Lys Met Leu Phe Tyr Lys Asp Gly Lys Pro Phe Arg Phe 35 40 45 Ser Ser Gln Asp Ser Glu Phe Thr Ile Leu Gln Thr Asn Leu Ser His 50 55 60 Asn Gly Ile Tyr His Cys Ser Gly Glu Arg Arg Arg 65 70 75 <210> SEQ ID NO 124 <211> LENGTH: 63 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 124 Pro Thr Gln Arg Glu Ala Met Thr Met Val Ala Ala Gln Val Met Gly 1 5 10 15 Asn His Val Gly Val Thr Asp Gly Gly Ser Asn Gly His Phe Glu Leu 20 25 30 Asn Val Phe Thr Pro Met Met Ile Lys Asn Val Leu His Ser Ala Arg 35 40 45 Leu Leu Gly Asp Ala Ser Ala Ser Phe Thr Glu Asn Cys Val Val 50 55 60 <210> SEQ ID NO 125 <211> LENGTH: 102 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 125 Met Arg Leu Ser Val Thr Ala Leu Leu Gly Thr Leu Ala Leu Cys Tyr 1 5 10 15 Tyr Lys Ala Asn Ala Ile Val Cys Pro Thr Phe Ala Ala Asp Leu Thr 20 25 30 Glu Phe Phe Tyr Phe Pro Asp Leu Leu Tyr Arg Leu Ser Leu Ala Lys 35 40 45 Tyr Asn Ala Pro Pro Glu Ala Val Ala Ala Lys Met Glu Val Lys Gln 50 55 60 Cys Thr Asp Arg Phe Ser Val Lys Asn Arg Leu Ile Ile Thr Asn Ile 65 70 75 80 Leu Gly Lys Ile Leu Leu Asn Cys Thr Val Thr Asp Val Lys Ala Val 85 90 95 Leu Asn Pro Ser Ser Ala 100 <210> SEQ ID NO 126 <211> LENGTH: 129 <212> TYPE: PRT <213> ORGANISM: Bovine <220> FEATURE: <221> NAME/KEY: VARIANT <222> LOCATION: (1)...(129) <223> OTHER INFORMATION: Xaa = Any Amino Acid <400> SEQUENCE: 126 Glu His His Tyr Arg Cys Val Val Gln His Ala Gly Leu Ala Gln Pro 1 5 10 15 Leu Thr Val Glu Leu Glu Ser Pro Ala Arg Thr Ser Val Pro Val Val 20 25 30 Gly Ile Val Ile Gly Leu Phe Leu Leu Leu Thr Val Ala Ala Gly Gly 35 40 45 Ala Leu Leu Trp Arg Arg Met Arg Lys Gly Leu Pro Ala Pro Trp Ile 50 55 60 Ser Phe Arg Gly Glu Asp Val Gly Ala Leu Leu Pro Thr Pro Gly Leu 65 70 75 80 Ser Lys Asp Gly Glu Ser Xaa Asp Lys Asn Ala Phe Pro Ala Thr Ala 85 90 95 Asp His Pro Pro Ser Trp Leu Leu Pro Ala Asn Val Leu Arg Ser Phe 100 105 110 Ser Cys Cys Glu Thr Ser Gly Asn Pro Gly Ile Phe Glu Pro Pro Glu 115 120 125 Gly <210> SEQ ID NO 127 <211> LENGTH: 46 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 127 Asn Gly Ser Ser Asp Trp Thr Gly Ser Ala Ala Asp Trp Thr Glu Gln 1 5 10 15 Ser Glu Leu Phe Arg Leu Leu Pro Ser Glu Leu Thr Leu Trp Val Asp 20 25 30 Pro Tyr Glu Val Ser Tyr Arg Ile Gly Glu Asp Gly Ser Ile 35 40 45 <210> SEQ ID NO 128 <211> LENGTH: 44 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 128 Gln Gln Thr Thr Asn Thr Val Glu Glu Pro Leu Asp Leu Ile Arg Leu 1 5 10 15 Ser Leu Asp Glu Arg Ile Tyr Val Lys Met Arg Asn Asp Arg Glu Leu 20 25 30 Arg Gly Arg Leu His Ala Tyr Asp Gln His Leu Asn 35 40 <210> SEQ ID NO 129 <211> LENGTH: 41 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 129 Phe Lys Arg Tyr His Asp Pro Asn Phe Val Pro Ala Ala Phe Val Cys 1 5 10 15 Ser Lys Cys Gly Lys Thr Phe Thr Arg Arg Asn Thr Met Ala Arg His 20 25 30 Ala Asp Asn Cys Ala Gly Pro Asp Gly 35 40 <210> SEQ ID NO 130 <211> LENGTH: 80 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 130 Glu Phe Gly Thr Ser Val Asn Ala Ala Gly Gly Pro Thr Pro Ser Gln 1 5 10 15 Arg Gly Leu Ser Asp Leu Ala Leu Cys Gly Pro Ala Ala Asn Gln Cys 20 25 30 Ala Val Pro Ala Lys Asp Arg Val Asp Cys Gly Tyr Pro Glu Val Thr 35 40 45 Pro Glu Gln Cys Asn Asn Arg Gly Cys Cys Phe Asp Ser Ser Ile His 50 55 60 Gly Val Pro Trp Cys Phe Lys Pro Leu Gln Glu Ala Glu Cys Thr Phe 65 70 75 80 <210> SEQ ID NO 131 <211> LENGTH: 69 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 131 Leu Pro Ser His Pro Ser Pro Gln Ser Arg Pro Leu Lys Thr His Glu 1 5 10 15 Leu Arg Asp Pro Val Leu Ser Ala Ala Ile Ala Thr Lys Met Ala Lys 20 25 30 Phe His Gly Met Glu Met Pro Phe Thr Lys Glu Pro His Trp Leu Phe 35 40 45 Gly Thr Met Glu Arg Tyr Leu Lys Gln Ile Gln Asp Leu Pro Pro Thr 50 55 60 Ser Leu Pro Gln Arg 65 <210> SEQ ID NO 132 <211> LENGTH: 141 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 132 Tyr Thr Arg Asp His Ala Gly Ser Phe Leu Thr Glu Ser Arg Ser Leu 1 5 10 15 Ser Thr His Leu Leu Leu Leu Tyr Gly Leu Gln Gly Leu Leu Thr Phe 20 25 30 Gly Tyr Leu Val Leu Leu Ser Arg Ile Gly Glu Arg Met Ala Val Asp 35 40 45 Leu Arg Arg Ala Leu Phe Cys Asn Leu Leu Arg Gln Asp Ile Glu Phe 50 55 60 Phe Asp Ala Lys Arg His Arg Leu Val Pro Gly Ala Leu Gln His Arg 65 70 75 80 Leu Gln Leu His Gly Leu Gly His Pro Val Cys Trp Gly Leu Thr Arg 85 90 95 Gly Arg Ala Ala Ala Asp Gly Gly Arg Pro His Val Leu Pro Gly Gly 100 105 110 Leu Ser Asp Cys Ala Glu Val Arg Val Gly Arg Ser Leu Pro Glu Gly 115 120 125 Pro Ser Trp Gly Arg Gly Arg Gln Ser Ser Val Asp Thr 130 135 140 <210> SEQ ID NO 133 <211> LENGTH: 41 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 133 Gly Thr Ser Ser Asn Pro His Thr Asp Thr Trp Lys Ser His Gly Leu 1 5 10 15 Val Glu Val Ala Ser Tyr Cys Glu Glu Ser Arg Gly Asn Asn Gln Trp 20 25 30 Val Pro Tyr Ile Ser Leu Gln Glu Arg 35 40 <210> SEQ ID NO 134 <211> LENGTH: 59 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 134 Leu Gly Asp Phe Phe Gly Asp Pro Gly Asn Pro Ser Ser Glu Phe Thr 1 5 10 15 Pro Ser Gly Ser Lys Asp Gly Lys Tyr Glu Leu Leu Thr Ala Ala Asn 20 25 30 Glu Val Ile Ala Glu Glu Ile Lys Asp Leu Met Thr Lys Ser Asp Ile 35 40 45 Glu Gly Gln His Thr Glu Thr Leu Leu Ala Gly 50 55 <210> SEQ ID NO 135 <211> LENGTH: 154 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 135 Ile Thr Cys Ser Gly Thr Ser Ser Asn Val Gly Asp Gly Asp Tyr Val 1 5 10 15 Ser Trp Phe Gln Gln Ile Pro Gly Ser Gly Pro Arg Thr Val Ile Phe 20 25 30 Gly Ala Thr Gln Arg Pro Ser Gly Val Ser Glu Arg Phe Ser Gly Ser 35 40 45 Arg Ser Gly Asn Thr Ala Thr Leu Thr Ile Ser Ser Leu Gln Ala Glu 50 55 60 Asp Glu Ala Asp Tyr Phe Cys Ser Ser Pro Asp Thr Thr Asn Asn Val 65 70 75 80 Ala Phe Gly Ser Gly Thr Thr Leu Ser Val Leu Arg Gln Arg Leu Glu 85 90 95 Ile Glu Arg Gln Leu Gln Leu Arg Gly His Ala Arg Arg Glu His Arg 100 105 110 Asp Glu Asp Ser Glu Ala Leu Arg Val Ser Leu Gly Pro Gly Pro Pro 115 120 125 Pro Ser Gly Ala Leu Trp Pro Thr Pro Pro Pro Pro Pro Leu His Gly 130 135 140 Pro Leu Ser Pro Tyr Pro Gly Arg Leu His 145 150 <210> SEQ ID NO 136 <211> LENGTH: 159 <212> TYPE: PRT <213> ORGANISM: Bovine <400> SEQUENCE: 136 Met Trp Gln Leu Leu Leu Pro Leu Ala Leu Gly Leu Gly Thr Met Gly 1 5 10 15 Leu Gly Arg Ala Glu Leu Thr Thr Ala Gln His Arg Gly Leu Gln Val 20 25 30 Ala Leu Glu Glu Phe His Lys His Pro Pro Val Leu Trp Ala Phe Gln 35 40 45 Val Thr Ser Val Asp Asn Ala Ala Asp Thr Leu Phe Pro Ala Gly Gln 50 55 60 Phe Val Arg Leu Glu Phe Lys Leu Gln Gln Thr Ser Cys Arg Lys Lys 65 70 75 80 Asp Trp Arg Lys Glu Asp Cys Lys Val Lys Pro Asn Gly Arg Lys Arg 85 90 95 Lys Cys Leu Ala Cys Ile Lys Leu Asp Ser Lys Asp Gln Val Leu Gly 100 105 110 Arg Met Val His Cys Pro Ile Gln Thr Gln Glu Leu Asp Asp Ala Gln 115 120 125 Asp Ala Gln Cys Ser Arg Val Glu Arg Ala Gly Glu Asp Pro His Ser 130 135 140 Tyr Tyr Leu Pro Gly Gln Phe Ala Phe Ile Lys Ala Leu Ser Pro 145 150 155 

We claim:
 1. An isolated polynucleotide comprising a sequence selected from the group consisting of: sequences recited in SEQ ID NOS: 1-68.
 2. An isolated polynucleotide comprising a sequence selected from the group consisting of: (a) complements of the sequences recited in SEQ ID NOS: 1-68; (b) reverse complements of the sequences recited in SEQ ID NOS: 1-68; and (c) reverse sequences of the sequences recited in SEQ ID NOS: 1-68; and (d) sequences that hybridize to a sequence recited in SEQ ID NOS: 1-68 under stringent hybridization conditions.
 3. An isolated polynucleotide comprising a sequence selected from the group consisting of: (a) sequences having at least a 99% probability of being the same as a sequence recited in SEQ ID NOS: 1-68; (b) sequences having at least 75% identity to a nucleotide sequence recited in SEQ ID NOS: 1-68; (c) sequences having at least 90% identity to a nucleotide sequence recited in SEQ ID NOS: 1-68; and (d) sequences having at least 95% identity to a nucleotide sequence recited in SEQ ID NOS: 1-68.
 4. An isolated polynucleotide comprising a sequence selected from the group consisting of: (a) nucleotide sequences that are 200 -mers of a sequence recited in SEQ ID NOS: 1-68; (b) nucleotide sequences that are 100 -mers of a sequence recited in SEQ ID NOS: 1-68; (c) nucleotide sequences that are 40 -mers of a sequence recited in SEQ ID NOS: 1-68; and (d) nucleotide sequences that are 20 -mers of a sequence recited in SEQ ID NOS: 1-68.
 5. An oligonucleotide comprising at least 10 contiguous residues complementary to 10 contiguous residues of a nucleotide sequence recited in SEQ ID NOS: 1-68.
 6. A genetic construct comprising an isolated polynucleotide of any one of claims 1-4.
 7. A host cell transformed with a genetic construct of claim
 6. 8. An isolated polypeptide encoded by a polynucleotide of SEQ ID NOS: 1-68.
 9. An isolated polypeptide comprising an amino acid sequence selected from the group consisting of: sequences provided in SEQ ID NOS: 69-136.
 10. An isolated polypeptide comprising an amino acid sequence selected from the group consisting of: (a) sequences having at least 75% identity to a sequence provided in SEQ ID NOS: 69-136; (b) sequences having at least 90% identity to a sequence provided in SEQ ID NOS: 69-136; and (c) sequences having at least 95% identity to a sequence provided in SEQ ID NOS: 69-136.
 11. An isolated polynucleotide encoding a polypeptide of any one of claims 9 and
 10. 12. An isolated polypeptide comprising at least a functional portion of a polypeptide of any one of claims 9 and
 10. 13. A composition comprising a polypeptide according to any one of claims 9 and 10 and at least one component selected from the group consisting of: physiologically acceptable carriers and immunostimulants.
 14. A composition comprising a polynucleotide according to any one of claims 1-3 and at least one component selected from the group consisting of pharmaceutically acceptable carriers and immunostimulants.
 15. A method for treating a disorder in a mammal comprising administering a composition according to claim
 13. 16. A method for treating a disorder in a mammal comprising administering a composition according to claim
 14. 17. A method for modifying mammary gland function, structure or composition in an organism, comprising transforming the organism with a genetic construct according to claim
 13. 18. A method for modifying mammary gland function, structure or composition in an organism, comprising administering a composition according to claim
 14. 19. A method for detecting the presence of mammary gland tissue in a biological sample, comprising: (a) contacting the biological sample with an oligonucleotide according to claim 5; (b) detecting in the sample the presence of a polynucleotide that hybridizes to the oligonucleotide.
 20. A diagnostic kit comprising at least one oligonucleotide according to claim
 5. 21. A transgenic organism comprising a host cell according to claim
 7. 